Method and apparatus for sterilizing preform

ABSTRACT

A method of sterilizing a preform includes steps of: sterilizing bacteria adhering to a preform ( 1 ) made of resin by gasifying a sterilizer, discharging a sterilized gas (G) from a nozzle ( 6 ) toward a preform ( 1 ), now traveling, so as to adhere to the preform ( 1 ); activating the sterilizer adhering to the preform ( 1 ) by blasting hot air (P) to the preform; and sterilizing bacteria adhering to the preform, and removing the sterilizer adhering to the preform ( 1 ), wherein the above steps are performed sequentially in order. According to the above-mentioned steps, the sterilizer does not enter a blow-molding machine.

TECHNICAL FIELD

The present invention relates to method and apparatus for sterilizing a preform.

BACKGROUND ART

In conventional art, there is provided a sterilizing method in which, while continuously conveying preforms, a sterilizer (sterilizing agent) is applied to the preforms, which are then introduced into a heating furnace, the preforms are heated in the heating furnace to a temperature suitable for forming the preform into a container, and during such heating, the sterilizer applied to the preform is dried and activated simultaneously (see Patent Documents 1, 2, 3).

Furthermore, there is also provided a drink filling method in which a preform is preheated, hydrogen peroxide mist or gas is blasted to the preheated preform, the preform is then heated to a temperature suitable for molding thereof, the preform of the suitable temperature for molding is molded into a bottle in a mold continuously traveling with the preform, the blow-molded bottle is taken out of the mold, and thereafter, the bottle is filled up with drink and then sealed with a lid (for example, Patent Documents 4, 5).

Still furthermore, there is also provided a method in which a preform is dipped into a sterilizing liquid to thereby sterilize the preform, the preform is heated to a temperature suitable for molding in a heating furnace after the sterilizer liquid adheres to the preform has been removed, and the preform is thereafter blow-molded into a container (see Patent Document 6).

PRIOR ART DOCUMENT Patent Document

Patent Document 1: Japanese Unexamined Patent Publication No. 2001-510104

Patent Document 2: Japanese Patent Laid-open Publication No. 2008-183899

Patent Document 3: Japanese Unexamined Patent Publication No. 2008-546605

Patent Document 4: Japanese Patent Laid-open Publication No. 2013-35561

Patent Document 5: Japanese Patent Laid-open Publication No. 2013-35562

Patent Document 6: Japanese Patent Laid-open Publication No. 04-44902

Problems to be Solved by the Invention

The conventional technologies described above concern to sterilization treatment of preforms before being molded to bottles. However, in such technologies, hydrogen peroxide adhering to the preform is introduced into a blow molding machine together with the preform, which may pose a fear such that the hydrogen peroxide introduced in the blow-molding machine will damage various members or components such as seal member within the blow-molding machine. In addition, in order to prevent the defective sterilization effect, if a lot of condensed mist of the hydrogen peroxide is blasted in the stage of the preform, the amount of the hydrogen peroxide adhering to the preforms may become uneven, and as a result, uneven heating may be caused to the preforms before the blow-molding process, which may produce defective product of bottle such as whitening (bleaching), distortion and other defective in the molding process.

The present invention aims to solve such problems as mentioned above.

Means for Solving the Problems

In order to solve the above problems, the present invention adopts the following configuration or structure.

It is further to be noted that although the description is made with parentheses to reference numerals for easy understanding of the invention, the present invention is not limited thereto.

That is, the invention defined in claim 1 adopts a method of sterilizing a preform, comprising the steps of: sterilizing bacteria adhering to the preform (1) made of resin by gasifying a sterilizer, discharging a sterilized gas (G) toward a preform, now traveling, so as to adhere to the preform by discharging the sterilizer from a nozzle; activating the sterilizer adhering to the preform (1) by blasting hot air (P) to the preform; and sterilizing the bacteria adhering to the preform (1) and removing the sterilizer adhering to the preform (1), wherein the above steps are performed sequentially in order.

As recited in claim 2, it may be preferred that, in the preform sterilizing method according to claim 1, the sterilizer is atomized in an evaporator (9) to be gasified as a gas, and the gas (G) is discharged toward the preform from a nozzle (6) of an evaporator (9).

As recited in claim 3, it may be preferred that, in the preform sterilizing method according to claim 1 or 2, at least one of nozzles (6) are disposed so as to face a preform traveling path and the sterilizer gas (G) is blasted toward the preform (1) from the nozzle (6).

As recited in claim 4, it may be preferred that, in the preform sterilizing method according to any one of claims 1 to 3, flow of the sterilizer gas (G) is branched into a plurality of flows, one of which flows toward a mouth portion (2 a) of the preform (1) and another of which flows toward an outer surface of the preform (1).

As recited in claim 5, it may be preferred that, in the preform sterilizing method according to claim 4, a surrounding of the one of sterilizer gas (G) flow discharged from the nozzle (6) is surrounded by an umbrella-shaped member (30), and gas or mist, or mixture thereof leaking from the mouth portion (2 a) of the preform (1) after entering the preform is guided by the umbrella-shaped member (30) to the outer surface of the preform (1).

As recited in claim 6, it may be preferred that, in the preform sterilizing method according to any one of claims 1 to 5, the sterilizer is a solution including at least 1% by mass of hydrogen peroxide component.

As recited in claim 7, it may be preferred that, in the preform sterilizing method according to any one of claims 1 to 4, foreign substance existing in the preform (1) is removed by a hot air (P).

As recited in claim 8, it may be preferred that, in the preform sterilizing method according to claim 1, an umbrella-shaped member (43 a) that covers above the mouth portion (2 a) of the preform (1) at a time when the preform is heated to a temperature for a blow-molding step.

As recited in claim 9, it may be preferred that, in the preform sterilizing method according to claim 1, an aseptic air (Q) is blasted to the mouth portion (2 a) of the preform (1) at a time when the preform (1) is conveyed toward the mold (4) after heating the preform (1) to the temperature for the blow-molding step.

The invention according to claim 10 adopts a preform sterilizing apparatus, including: a traveling unit that transfers a preform (1) or a bottle (2) from a supplying stage of the preform to a molding stage of the bottle; a nozzle (6) that supplies a sterilizer gas (G) to the preform (1); and an air nozzle (80) that activates the sterilizer adhering to the preform (1) by blasting a hot air (P) to the preform (1) and removes the sterilizer adhering to the preform therefrom, wherein the sterilizer gas supplying nozzle (6), and the hot air supplying nozzle (80) are arranged in subsequently from an upstream side toward a downstream side of the traveling unit.

As recited in claim 11, it may be preferred that, in the preform sterilizing apparatus according to claim 10, the sterilizer atomized by a spray nozzle (8) is gasified into a gas (G), and a nozzle (6) is arranged to a front end portion of an evaporator (9) from which the gas (G) is discharged toward the preform (1).

As recited in claim 12, it may be preferred that, in the preform sterilizing apparatus according to claim 10 or 11, the nozzle (6) that supplies the sterilizer is disposed along a preform traveling path, and the sterilizer gas (G) is discharged toward the preform (1) from the nozzle (6).

As recited in claim 13, it may be preferred that, in the preform sterilizing apparatus according to any one of claims 10 to 12, the sterilizer gas supplying nozzle (6) is branched into a plurality of pipe lines (6 a, 6 b), one (6 a) of the pipe lines has a discharge port facing an opening of the preform so that a discharge port faces the outer surface of the preform, and another pipe line (6 b) extends toward the outer surface of the preform (1) so that a discharge port (31) thereof faces the outer surface of the preform (1).

As recited in claim 14, it may be preferred that, in the preform sterilizing apparatus according to claim 13, a surrounding of the one (6 a) of the pipe line is surrounded by an umbrella-shaped member (30), and gas or mist, or mixture thereof leaking from the mouth portion of the preform after entering the preform is guided by the umbrella-shaped member (30) to the outer surface of the preform (1).

As recited in claim 15, it may be preferred that, in the preform sterilizing apparatus according to any one of claims 10 to 14, the sterilizer is a solution including at least 1% by mass of hydrogen peroxide component.

As recited in claim 16, it may be preferred that, in the preform sterilizing apparatus according to claim 10, the air nozzle (80) is provided with a blasting port (80 a) in form of slit for blasting the hot air (P) and the blasting port (80 a) extends along the traveling direction of the preform (1).

The air nozzle (80) may be disposed for supplying the hot air (P) to the outer surface of the preform (1). According to such supplying, the sterilizer adhering to the outer surface of the preform (1) can be removed. Further, a plurality of air nozzles (80) may be also provided, around a conveying wheel (16), each in a tubular shape so as to perform a turning motion following the preform (1).

As recited in claim 17, it may be preferred that, in the preform sterilizing apparatus according to any one of claims 10 to 16, a foreign substance exiting in the preform (1) is removed by the hot air (P).

As recited in claim 18, it may be preferred that, in the preform sterilizing apparatus according to claim 10, an umbrella-shaped member (43 a) that covers above the mouth portion (2 a) of the preform (1) is provided within the heating furnace (33).

As recited in claim 19, it may be preferred that, in the preform sterilizing apparatus according to claim 10, a cover (86) is arranged on a way of a bottle traveling path along which the preform (1) travels from the heating furnace (33) to the mold (4) for blow-molding, and an aseptic air (Q) is blasted from the cover side toward the mouth portion (2 a) of the preform (1).

Effects of the Invention

The present invention is a method of sterilizing a preform including the steps of: sterilizing bacteria adhering to a preform (1) made of resin by gasifying a sterilizer, discharging a sterilized gas (G) toward a preform, now traveling, so as to adhere to the preform by discharging the sterilizer from a nozzle; activating the sterilizer adhering to the preform (1) by blasting hot air (P) to the preform; sterilizing the bacteria adhering to the preform (1), and removing the sterilizer adhering to the preform (1), wherein the above-mentioned steps are performed subsequently in order. Thus, according to the present invention, the preform (1) can be conveyed into the blow-molding machine (12) by removing surplus sterilizer such as hydrogen peroxide supplied into the preform (1). Accordingly, the sterilizer can be blocked from entering the blow-molding machine (12) to thereby prevent damage to various components in the blow-molding machine by the sterilizer.

Furthermore, since any sterilizer does not adhere to the preform (1) entering the blow-molding machine (12), molding defects such as bleaching, distortion, whitening, uneven molding and the like defective can be prevented from causing at the molding treatment of the bottle (2).

Still furthermore, since the hot air (P) is blasted to the preform (1) after supplying the sterilizer, the sterilizer adhering to the preform (1) is activated, and hence, bacteria adhering to the preform (1) can be effectively sterilized, the sterilizing performance can be improved, and the sterilizing effect to the bottle (2) manufactured from the preform (1) can be also improved.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 represents a preform sterilizing method according to a first embodiment 1 of the present invention, in which (A), (B), and (C) show a hydrogen peroxide supply process to a preform, a hot-air supply process performed to the preform, and a heating process to the preform, respectively.

FIG. 2 includes (D), (E), (F), and (G) representing a preform molding process, a bottle take-out process, a content filling process, and a sealing process, respectively.

FIG. 3 is a plan view illustrating one example of an aseptic filling system equipped with a preform sterilizing apparatus according to the present invention.

FIG. 4 is a vertical sectional view illustrating one example of a sterilizing gas generator for generating a hydrogen peroxide gas.

FIG. 5 shows an air nozzle to be incorporated in the preform sterilizing apparatus according to the present invention, in which (A) is a plan view thereof and (B) is a vertical sectional view thereof.

FIG. 6 is a vertical sectional view illustrating a hydrogen peroxide supply nozzle incorporated in the preform sterilizing apparatus according to the present invention.

FIG. 7 is a view explaining a modified example showing hot air blasting process to the preform.

FIG. 8 is a view explaining another modified example showing hot air blasting process to the preform.

FIG. 9 is a view explaining a further modified example showing hot air blasting process to the preform.

FIG. 10 represents a preform sterilizing method according to a second embodiment 2 of the present invention, in which (A), (B), and (C) show a hydrogen peroxide supply process to a preform, a hot-air supply process to the preform, and a heating process to the preform, respectively.

FIG. 11 includes (D), (E), and (F) representing an aseptic air blasting process to a preform, a bottle molding process to the preform and an aseptic air blasting process to the bottle, respectively.

FIG. 12 includes (G), (H1), and (H2), in which (G) shows a hydrogen peroxide supply process to the bottle, and (H1) or (H2), which represent a hot water rinsing process, a content filling process, and a sealing process, respectively, after the hydrogen peroxide supply process.

FIG. 13 includes (I), (J), and (K), which illustrate a hot water rinsing process, a content filling process and a sealing process, respectively, after the hydrogen peroxide supply process.

FIG. 14 is a plan view illustrating another example of an aseptic filling system incorporating the preform sterilizing apparatus.

FIG. 15 is a vertical sectional view showing a nozzle for blasting the hot air into the preform in FIG. 10(C).

FIG. 16 is a vertical sectional view of a nozzle used in place of the sterilizer supply nozzle shown in FIG. 6.

FIG. 17 is a view illustrating a modified example of the aseptic air supply process.

FIG. 18 is a plan view showing an aseptic filling system incorporating the process shown in FIG. 17.

FIG. 19 is a view illustrating another modified example of the aseptic air supply process.

FIG. 20 is a plan view illustrating the aseptic filling system incorporating the process shown in FIG. 19.

FIG. 21 is a plan view showing a further example of an aseptic filling system incorporating the preform sterilizing apparatus.

EMBODIMENT FOR CARRYING OUT THE INVENTION

Hereunder, embodiments for carrying out the present invention will be explained.

First Embodiment 1

According to this first embodiment, by sterilizing a preform, a bottle can be manufactured as sterilized one, the bottle can be filled with an aseptic drink, the bottle is then sealed with an a sterilized lid, and thereafter, the bottle is manufactured as finally packaged product such as shown in FIG. 2(G).

The packaged product is constructed with an aseptic (i.e., sterilized) bottle 2 and a cap 3 as a lid.

In this embodiment, although the bottle is made of PET (polyethylene terephthalate), the bottle is not limited to the PET, and it is made of a resin material such as polypropylene, polyethylene or like resin, and a re-cycled PET allocated resin may be also used. Further, a male screw (i.e., thread) is formed to a mouth portion 2 a of the bottle 2.

The cap 3 is made up from a resin material such as polyethylene by an injection molding or like process or like, and a female (thread) portion is formed to an inner peripheral surface of the cap 3 at the same time for molding the cap 3.

The bottle 2 is filled up with drink “a” which has been preliminarily sterilized in a state that the interior of the bottle has been preliminarily sterilized. The cap 3 is applied to the mouth portion 2 a of the bottle 2 after the filling of the drink “a”, and then fastened and sealed thereto through screw-engagement between the male and female threads, thus completing a packaged product. The cap 3 is also preliminarily sterilized.

The bottle 2 is formed as a packaged product through the sterilizing process, the molding process, the drink filling process and the sealing process.

First, a preform 1 shown in FIG. 1(A) is continuously delivered at a predetermined speed.

The preform 1 is formed as a bottomed tubular member such as test tube by injection-molding the PET. The preform 1 is formed with a mouth like the mouth portion 2 a of the bottle 2 shown in FIG. 2(G) at the initial time of the molding. The mouth portion 2 a is also formed with a male thread at the same time of molding the preform 1.

As shown in FIG. 1(A), a sterilizer gas G or mist, or mixture thereof is supplied to the preform 1 in a state of being conveyed and held by a gripper 32.

In the present embodiment, although a hydrogen peroxide is used in the present embodiment as a sterilizer gas (sterilizing agent), another sterilizer or sterilizing agent is also usable.

As shown in FIG. 1(A), the preform 1 is blasted with the hydrogen peroxide gas G as a sterilizer through a sterilizer supplying nozzle 6.

The hydrogen peroxide gas G is divided into two flows within the sterilizer supplying nozzle 6, and one of them is jetted toward inside the preform 1 and the other one is jetted toward an outer surface of the preform 1. After the hydrogen peroxide gas G is blasted through the sterilizer supplying nozzle 6, it flows into the preform in a state of gas, mist, or mixture thereof, or it flows in contact to the outer surface of the preform 1.

Further, an outside of the flow of the gas G jetted toward inside the preform is covered by an umbrella-shaped member 30. Although the gas G or mist flowing into the preform 1 leaks out of the mouth portion 2 a of the preform 1, the flow of the leaking gas G or like collides with the umbrella-shaped member 30, is guided along the inner surface thereof, changes its flow direction towards the outer surface thereof, and contacts the outer surface of the preform 1.

As mentioned above, the hydrogen peroxide gas G, mist of their mixture contacts the inner and outer surfaces of the preform 1 and adheres thereto, thereby sterilizing bacteria or like adhering to the surface of the preform 1 or being damaged.

Further, immediately before the blasting of the hydrogen peroxide gas G to the preform 1 shown in FIG. 1(A), the preform may be preliminarily heated by blasting hot air thereto. According to such preheating, the sterilizing effect to the preform can be further enhanced.

The hydrogen peroxide gas G blasted to the preform 1 is generated by a sterilizer gas generator 7, which will be explained hereinafter with reference to FIG. 4. The hydrogen peroxide gas G flows out of the sterilizer supplying nozzle 6, contacts the inner and outer surfaces of the preform 1, and adheres as a condensed film of the hydrogen peroxide 35% by mass reduction with a thickness of preferably 0.001 μL/cm² to 0.5 μL/cm².

In a case when the adhering amount of the hydrogen peroxide is less than of 0.001 μL/cm², sufficient sterilizing effect will not be expected, and in a case when the adhering amount thereof is more than 0.05 μL/cm², molding defect such as whitening (bleaching), spot generation, wrinkling formation, deformation and the like will be liable to be caused when the preform 1 is molded into the bottle 2 as shown in FIG. 2(D).

The adhering amount of the condensed film of the hydrogen peroxide reduced with 35% by mass to the preform 1 is more preferably 0.002 μL/cm² to 0.4 μL/cm².

As mentioned above, in the case when the hydrogen peroxide gas G is supplied to the preform 1 to thereby adhere the condensed film on the surface of the preform 1, since the condensed film of the hydrogen peroxide is rapidly condensed and concentrated on the preform 1, which leads to the improved sterilization effect to the surface of the preform 1. In addition, according to such improvement of the sterilization effect, the amount of the hydrogen peroxide to be used for the sterilization can be reduced, and hence, the possibility of remaining of the hydrogen peroxide on the surface of the preform 1 will be also reduced.

Further, it may be possible to preheat the preform 1 by blasting the hot air or like just before the blasting of the hydrogen peroxide to the preform shown in FIG. 1(A). According to such preheating, the sterilizing effect to the preform can be further enhanced.

A plurality of sterilizer supplying nozzles 6 may be arranged, other than only one, along the traveling path of the preform to effectively blast the sterilizer gas from the plural sterilizer supplying nozzles 6 toward the preform 1.

Subsequently, as shown in FIG. 1(B), to the preform 1 supplied with the hydrogen peroxide, the hot air P is supplied from an air nozzle 80 while being conveyed by the gripper 32.

According to such blasting of the hot air P, the hydrogen peroxide adhering to the surface of the preform 1 is activated by the heat of the hot air P, thereby sterilizing bacteria or like in the preform 1. Furthermore, the hydrogen peroxide adhering on the preform 1 can be promptly rejected from the surface of the preform 1 by blasting the hot air P.

As shown in FIG. 1(B), the hot air P is blasted through a slit-shaped blasting port 80 a formed to a box-shaped manifold 80 b constituting the air nozzle 80, but the hot air P may be blasted from a tubular blasting nozzle 81 toward the preform 1 as shown in FIG. 7. Moreover, it may be possible to arrange a suction tube 82 near the blasting nozzle 81 so as to suck foreign substance or material such as dust exhausted outside from the preform 1 by the suction tube 82 at a time of blasting the hot air P from the tubular blasting nozzle 81 into the preform 1. As mentioned above, by recovering the foreign substance by the suction tube 82, the foreign substance can be prevented from mixing into the other preform or bottle formed thereafter.

Further, as shown in FIG. 8, it may be possible to dispose the blasting nozzle 81 blasting the hot air P with an opening directed upward and with the preform in the inverted state, in which the hot air P is blasted into the preform 1 through the mouth portion 2 a from the lower side of the blasting nozzle 81 of the inverted preform 1. According to such arrangement, the foreign substance existing inside the preform 1 can be removed from the preform 1 by blasting air under pressure through the mouth portion 2 a as well as self-gravity thereof.

At the instance of ending the hot air blasting, the sterilization to the preform 1 is also ended. The thus sterilized preform 1 is stored in a container, not shown, in an aseptic state, or conveyed to the blow-molding step subsequently performed as mentioned hereunder (after FIG. 1(C)).

In a case when the preform having been subjected to the sterilizing treatment is immediately conveyed to the blow-molding step, the preform 1 is, as shown in FIG. 1(C), heated to a temperature suitable for the following blow-molding process by the infrared heater 18 a or other heating means. This temperature is within 90° C. to 130° C.

Further, a temperature for heating the mouth portion 2 a of the preform 1 is suppressed to a temperature less than 70° C. for preventing deformation or like of the preform.

When a process progresses to such heating process as mentioned above, the preform 1 is released from the gripper 32, and it is desirable, as shown in FIG. 1(C), to insert a spindle (or mandrel) 43 into the mouth portion 2 a to be thereby conveyed while rotating together with the spindle (mandrel) in a suspended upstand state (or upside down state). Thus, the preform 1 can be evenly heated by the infrared heater 18 a.

It may be possible to insert the mandrel in place of the spindle 43 into the preform 1 so as to convey the preform while rotating in the inverted (upside down) state.

The heated preform 1 is released from the spindle, and as shown in FIG. 2(D), is blow-molded into the bottle 2 within the mold 4.

The mold 4 for the blow-molding travels continuously at the same speed as the traveling speed of the preform, and is then clamped (mold-clamped). Thereafter, the mold 4 is opened after the blow-molding process is performed to the preform 1 within the mold 4.

As mentioned above, the preform 1 is entirely, except its mouth portion 2 a, uniformly heated to a temperature suitable for the heating process shown in FIG. 1(C), the thus heated preform 1 is placed and set in the mold 4 as shown in FIG. 1(D), and an extension rod (not shown) is inserted into the preform 1 through a center hole of the blow nozzle 5.

During the traveling of the mold 4, the preform 1 is expanded into the bottle 2 as final product within a cavity C of the mold 4 by sequentially blasting aseptic air, for example, for primary blow-molding and for secondary blow-molding from the blow nozzle 5 into the preform 1.

When the bottle 2 has been molded in the mold 4, the mold 4 is opened while being transferred, and the final product of the bottle 2 is taken out of the mold by the gripper 32 as shown in FIG. 2(E).

The bottle 2 taken out of the mold 4 is filled up with the drink “a” through the filling nozzle 10 as shown in FIG. 2(F) while being held by the gripper 32, and subsequently, as shown in FIG. 2(G), the cap 3 as a lid is applied to the bottle 2.

Further, the drink “a” may fill the bottle 2 at a normal temperature under an aseptic environment after the sterilizing treatment subjected to the drink itself.

Otherwise, as shown in the following Table 1, the drink “a” may fill the bottle 2 at a medium temperature such as 60 to 75° C.

In a case of no use of a past riser or a past cooler, sufficient sterilizing effect can be obtained by filling the bottle 2 at a temperature of more than 70° C. in an assumption of an outside temperature of 3° C.

On the other hand, in a case of use of a pasteurizer or a pasteu-cooler, a predetermined desirable sterilizing effect against mold spore can be obtained by treating the temperature of the pasteurizer for 5 to 10 minutes at a temperature of more than 60 to 65° C.

Further, in a case when the drink temperature at the filling time is more than 75° C., although the sufficient sterilizing effect can be obtained, if the bottle is made of PET, there is a fear such that the bottle is deformed except a case of a heat-resisting PET bottle, so that a test was conducted at temperatures under 75° C.

TABLE 1 use of pasteurizer or pasteu-cooler no use of hot water shower hot water shower pasteurizer or temperature temperature pasteu-cooler drink 65.0° C. 60.0° C. (constant temperature shower shower shower shower temperature at filling time time time time chamber time 10 min 5 min 10 min 5 min of 3° C.) 75.0° C. — — — — ◯ 72.5° C. — — — — ◯ 70.0° C. — — — ◯ ◯ 65.0° C. — ◯ ◯ Δ X 60.0° C. — ◯ Δ X — 55.0° C. — X X X —

Further, in the above Table 1, [◯] represents a case of sterilizing effect of more than 6.0 Log, [Δ] represents a case of sterilizing effect of 5.5 Log to 6.0 Log, and [x] represents a case of sterilizing effect of less than 5.0 Log.

The above test was conducted for the purpose of obtaining a condition for a filling temperature of drink which can achieve the sterilizing effect of more than 6.0 Log with respect to fungus (mold) of A. niger NBRC6341 as to a bottle inner surface and a cap inner surface. Further, although another fungus having a heat resisting property more than that of this fungus exists, in view of the sterilizing effect to the preform by chemical agent sterilization and the sterilizing effect to the chamber by SOP treatment, it is considered that commercially suitable aseptic filling operation may be performed by ensuring the sterilizing effect of 6 Log.

The test was conducted in a condition such that a hot water filled a fungus adhering bottle, an inverted sterilization was performed for 30 seconds after the filling, and subsequently, the filled water was filtrated by a filter and then cultivated. Thereafter, liquid culture medium was mixed and diluted, and was then separately cultivated.

In the filling case at the medium temperature, although the remaining of spore fungus in the drink “a” or bottle 2 is permitted, mold, yeast or like fungus is sterilized by the heat of the drink “a”, and the deformation of the PET bottle 2 is not permitted to be deformed. Accordingly, the case of the middle temperature filling treatment is suitable for acidic drink, carbonated drink, mineral water, which have the nature of suppressing germination of spore fungus, or neutral drink which is proven to a hot pack.

The aseptic filling system for performing the sterilizing treatment to the preform as mentioned above is constructed as one shown in FIG. 3, for example.

As shown in FIG. 3, the aseptic filling system includes a preform supply machine 11 for sequentially supplying preforms 1, each having a bottomed tubular shape, a blow-molding machine 12, and a filling machine 13 for filling a molded bottle 2 with the drink “a” and sealing the same with a cap 3 (see FIG. 2(G)).

The aseptic filling system is surrounded by chambers 41 a, 41 b, 41 c and 41 d at several portions on the way between the blow-molding machine 12 and the filling machine 13. The chamber 41 b may be mere a frame structure such as shroud with no sealing structure.

Further, it is possible to manufacture a bottle having high aseptic condition level by sterilizing the chamber 41 b before the manufacture of a package and supplying positive pressure passing through an HEMA filter into the chamber 41 b to thereby maintain the aseptic condition in the chamber 41 b. As one of such sterilizing method, the interior of the chamber 41 b may be sterilized by the hydrogen peroxide gas of less than 10 mg/L, or portions to which the preform 1 and the bottle 2 contact may be irradiated with a UV lamp (for ultraviolet ray sterilization). Furthermore, portions, to which a mold, an extension rod, a gripper and the like contact, may be wiped up with a chemical agent containing 1% by mass of ethanol or hydrogen peroxide.

A preform conveying means, a mold conveying means and a bottle conveying means are located on the way between the preform supplying machine 11 and the filling machine 13, in which the mold conveying means is for conveying the preforms 1 on the first conveying path, the mold conveying means is for conveying the mold 4 having a cavity “C” having a shape corresponding a final product of the bottle 2 (see FIG. 2(D)) on the second conveying path connected to the first conveying path, and the bottle conveying means is for conveying the bottle 2 molded by the mold 4 on the third conveying path connected to the second conveying path.

The first conveying path for the preform conveying means, the second conveying path for the mold conveying means and the third conveying path for the bottle conveying means are communicated with each other, and the grippers 32 and like members, not shown, for holding and conveying the preforms 1 and the bottles 2 are provided on these conveying paths.

The preform conveying means is provided, on its first conveying path, with a preform conveyer 14 for subsequently conveying the preforms 1 at a predetermined interval. The preform conveying means is further provided with a line (train) of wheels 15, 16, 17 which receive the preforms 1 from the terminal end of the conveyer 14, and an endless chain 18 which receives the preforms 1 and then conveys the preforms 1.

A sterilizer gas generator 7 generating the hydrogen peroxide gas G and a sterilizer supplying nozzle 6 for discharging the hydrogen peroxide gas G toward the preform 1 are located on predetermined positions on the traveling path of the preform 1 in the wheel 15.

As shown in FIG. 4, the sterilizer gas generator 7 is provided with a hydrogen peroxide supplying portion 8 constructed as a twin-fluid spray nozzle for supplying the solution of the hydrogen peroxide as the sterilizer in form of liquid drops and an evaporating portion (evaporator) 9 for evaporating the hydrogen peroxide by heating the mist of the hydrogen peroxide supplied from the hydrogen peroxide supplying portion 8 to a temperature more than its boiling point and less than its non-degradable temperature. The hydrogen peroxide supplying portion 8 has a structure in which the hydrogen peroxide solution from a hydrogen peroxide supply path 8 a and compressed air from a compressed air supply path 8 b respectively introduced into the hydrogen peroxide supplying portion 8 are then atomized into the evaporating portion 9. The evaporating portion 9 is in form of a pipe with a heater 9 a interposed between inner and outer wall portions thereof, and the hydrogen peroxide mist sprayed into this pipe is heated and then evaporated. The evaporated hydrogen peroxide gas is jetted outward of the evaporating portion 9 through the sterilizer supply nozzle 6.

As shown in FIG. 6, the sterilizer supply nozzle 6 is branched into a plurality of pipe lines 6 a, 6 b for sending the hydrogen peroxide gas G.

The pipe line 6 a among the plural pipe lines 6 a, 6 b has a discharge port facing an opening of the mouth portion 2 a of the preform 1. The hydrogen peroxide gas G generated by the sterilizer gas generator 7 is blasted toward the preform 1 from the discharge port of the pipe line 6 a of the sterilizer supply nozzle 6 in form of gas G or mist, or mixture thereof, and flows into the preform 1. In this manner, the hydrogen peroxide adheres to the inner surface of the preform 1 to thereby sterilize bacteria and the like fungus adhering to the inner surface of the preform.

Further, by supplying hot air, as aseptic air, into the sterilizer supply nozzle 6, the pipe lines 6 a, 6 b and others from middle portions thereof, dew condensation of the hydrogen peroxide solution in these pipe lines may be prevented. Such dew condensation may also be prevented by winding electric ribbon heater around the pipe lines 6 a, 6 b and the others.

It is preferred that a portion around the discharge port of the pipe line 6 a is covered with an umbrella-shaped member 30, which has a lower surface in which an annular groove 30 a having approximately semi-circular section is formed. The hydrogen peroxide gas G or mist, or their mixture flowing into the preform 1 through the discharge port of the pipe line 6 a fills the preform 1, and thereafter, leaks outward. However, the leaked hydrogen peroxide gas G or mist, or their mixture is guided to the outer surface of the preform 1 by the lower surface of the umbrella-shaped member 30 and the annular groove 30 a and then flows outward along the outer surface of the preform 1. Accordingly, the hydrogen peroxide leaking from the pipe line 6 a also adheres to the outer surface of the preform 1.

On the other hand, the other pipe line 6 b is formed so as to extend in an approximately U-shape along the outer surface of the preform 1, and a discharge port 31 of this pipe line 6 b faces the outer surface of the preform 1. The hydrogen peroxide gas G generated by the sterilizer gas generator 7 is jetted toward the outer surface of the preform also from the discharge port 31 of the other pipe line 6 b, and the thus formed hydrogen peroxide gas G or mist, or their mixture is blasted to the outer surface of the preform 1. The blasted hydrogen peroxide from the pipe line 6 a is mixed with the hydrogen peroxide leaking from the mouth portion 2 a of the preform 1 and adheres to the outer surface of the preform, thereby sterilizing bacteria and the like fungus adhering to the outer surface of the preform 1.

The amount of the hydrogen peroxide solution to be blasted to the inner and outer surfaces of the preform 1 can be adjusted by respectively adjusting the inner diameter of the discharge port 31 of the pipe line 6 a for supplying the gas G to the inner surface of the preform 1, the inner diameter of the discharge port 31 of the pipe line 6 b, the number of the discharge ports and the like.

An air nozzle 80 (FIG. 1(B)) is disposed on the traveling path of the preform 1 in the wheel 16, the air nozzle 80 acting to activate the hydrogen peroxide adhering to the inner and outer surfaces of the preform 1 by discharging the hot air P toward the preform 1 to thereby discharge the activated hydrogen peroxide externally of the preform 1.

As shown in FIG. 5(A), the air nozzle 80 has a box-shaped manifold 80 b bent along a circular arc of the wheel 16, and the blasting port 80 a in form of slit is formed in the bottom surface of the manifold 80 b. The air nozzle 80 is located above the wheel 16 so that the blasting port 80 a of the air nozzle 80 extends along the traveling path of the preform 1 in the wheel 16. Furthermore, as shown in FIG. 5(B), a blower 76, an HEPA filter 77, and an electric heater 78 are connected in series to the manifold 80 b. Outside air taken by the blower 76 is sterilized by the HEPA filter 77 and then heated by the electric heater 78 to generate the hot air P which is then send into the air nozzle 80.

Air to be supplied to the air nozzle 80 may be a compressed air which has a high propelling force and is sterilized by an aseptic filter without using the air from the blower 76. Moreover, a highly pressurized air using for blow-molding in the blow molding machine 12 may be re-used by being recovered.

The hot air P supplied into the manifold 80 b of the air nozzle 80 is jetted from the blasting port 80 a, flows toward the preform 1 traveling under the blasting port 80 a with the mouth portion 2 a thereof being directed upward, and a part of the hot air P flows into a hollow interior of the preform 1 and the other part thereof flows along the outer surface of the preform 1.

The hydrogen peroxide adhering to the inner and outer surfaces of the preform 1 is activated by the heat of the hot air P, and the bacteria and other fungus adhering to the preform 1 can be thereby sterilized. Furthermore, surplus hydrogen peroxide is removed from the preform 1, and the intrusion of the hydrogen peroxide into the subsequent heating furnace 33 can be prevented.

Further, the foreign substance removing percentage or ratio can be increased by arranging a suction tube 82 as shown in FIG. 7 and inverting the nozzle 81 and the preform 1 as shown in FIG. 8.

The supply of the hot air P may be performed by using an air nozzle 83 shown in FIG. 9. The air nozzle 83 has a structure similar to that of the sterilizer supply nozzle shown in FIG. 6. In FIG. 9, reference numerals 83 a and 83 b denote a plurality of blanched pipe lines for sending the hot air P, in which a discharge port of one pipe line 83 a faces the opening of the mouth portion 2 a of the preform. The hot air P is jetted from the discharge port of the pipe line 83 a toward the preform 1 and flows into the preform 1. As a result, the hydrogen peroxide adhering to the inner surface of the preform 1 is activated and the surplus hydrogen peroxide is removed.

Reference numeral 84 denotes an umbrella-shaped member covering the periphery of the discharge port of the pipe line 83 a, and an annular groove 84 a having approximately semi-circular sectional shape is formed in the lower surface of the umbrella-shaped member 84. The hot air P introduced into the preform 1 from the discharge port of the pipe line 83 a fills the interior of the preform 1, and then, leaks from the mouth portion 2 a of the preform 1. The leaking hot air P is guided to the outer surface of the preform 1 by the lower surface of the umbrella-shaped member 84 and the annular groove 84 a and flows along the outer surface of the preform 1 so that the hot air P leaking from the pipe line 83 a also contacts the outer surface of the preform 1.

On the other hand, the other pipe line 83 b is formed so as to extend in an approximately U-shape along the outer surface of the preform 1, and a discharge port 85 of this pipe line 83 b faces the outer surface of the preform 1. The hot air P is jetted toward the outer surface of the preform 1 also from the discharge port 85 of the other pipe line 83 b and contacts the outer surface of the preform 1. As a result, the hot air P from the pipe line 83 a is mixed with the hot air P leaking from the mouth portion 2 a of the preform 1 and adheres to the outer surface of the preform 1. Then, the hydrogen peroxide adhering to the outer surface of the preform 1 is activated, and the surplus hydrogen peroxide is removed.

As shown in FIG. 3, the wheels 15 and 16 are surrounded by the chamber 14 a, to which exhaust means composed of a filter 36 for filtrating the air inside the chamber 41 a and a blower 37 is connected. According to such connection, the surplus hydrogen peroxide discharged from the sterilizer supply nozzle 6 is removed by the filter 36 of the exhaust means, and thereafter, is discharged outside the chamber 41 a. Thus, the flow-in of the hydrogen peroxide into the adjacent blow-molding machine 12 can be prevented. It is preferred to adjust the supply amount into or exhaust amount from the chamber 41 a so as to create a negative pressure in the chamber 41 a lower than atmospheric pressure.

Further, bacteria or like fungus may be prevented from invading into the chamber 41 a now under negative pressure by locating the chamber 41 a, the heating furnace 33, the chamber 41 b and so on within a clean room, not shown, such as chamber 41 b.

The endless chain 18 is disposed as the conveying path of the preforms 1 within the heating furnace 33 provided with the infrared heater 18 a described above. A number of spindles 43 shown in FIG. 1(C) ate attached to the endless chain 18 at a constant pitch. Each spindle 43 can rotate while traveling together with the traveling of the endless chain 18. Into the mouth portion 2 a of the preform 1 delivered to the endless chain (18) side from the wheel (17) side, the spindle 43 is inserted as shown in FIG. 1(C), so that the preform 1 can be kept in its positively standing attitude. It may be further possible to convey the preform in the standing attitude as shown in FIG. 8 by replacing the spindle with a mandrel.

The heating furnace 33 is provided with a furnace chamber extending in one direction. Inside the furnace chamber, the endless chamber 18 is stretched between a pair of pulleys 34 a and 34 b opposing to each other in a horizontal plane. The endless chain 18 and associated members constitute an endless conveyer for conveying a number of the preforms 1 in a suspended attitude. The infrared heaters 18 a are attached to the inner peripheral wall of the furnace chamber along the outward path and return path of the traveling of the endless chain 18.

When the preform 1 is received by the spindle 43 through the preform conveyer 14 and the row of the wheels 15, 16 and 17, the preform 1 rotates and travels along the inner wall surface of the heating furnace 33. The infrared heaters 18 a are attached throughout the inner wall surface of the heating furnace 33, so that the preform 1 conveyed by the spindle 43 is heated by these infrared heaters 18 a. The preform 1 rotates in the heating furnace 33 together with the rotation of the spindle while being evenly heated by the infrared heaters 18 a, and portions other than the mouth portion 2 a of the preform 1 are heated up to a temperature 90° C. to 130° C. suitable for the blow-molding. The heating temperature to the mouth portion 2 a is regulated to less than 70° C. so as not to damage the sealing performance and not to deform the preform 1 when the cap is applied to the mouth portion 2 a.

The blow-molding machine 12 is provided with several sets of the mold 4 and the extension rods (FIG. 2(D)) for receiving the preform heated by the infrared heater 18 a of the preform supplying machine 11 and then molding the preform 1 into the bottle 2.

As shown in FIG. 3, the second conveying path of the mold conveying means is located within the blow-molding machine 12. The second conveying path is composed of a line of wheels 19, 20, 21 and 22.

A plurality of molds 4 and extension rods 5 are located around the wheel 20, and turn around the wheel 20 at a constant speed together with the wheel 20.

When the gripper, not shown, of the wheel 19 receives the preform 1 heated in the heating furnace 33 of the preform supplying machine 11 and then transfers the preform 1 to the mold 4 located around the wheel 20, the mold 4 now being opened in two mold halves is closed to thereby grip the preform 1 such as shown in FIG. 2(D). The preform 1 in the mold 4 is blown with highly pressurized air through an aseptic filter for blow-molding from the slit-shaped nozzle, not shown, located near the extension rod 5 while being rotated around the wheel 20 together with the mold 4 and the extension rod 5, thereby molding the preform as a final product of a bottle 2. As shown in FIG. 1(C), since the preform 1 is heated evenly to a predetermined temperature within the heating furnace 33, the blow-molding process can be smoothly performed.

Furthermore, as described above, the hydrogen peroxide adhering to each preform 1 is removed from the preform 1 before the entrance into the heating furnace 33 by blowing the hot air P. Accordingly, the seal member and other components or members located inside the blow-molding machine 12 becomes free from any damage by the adhesion of the hydrogen peroxide. Moreover, whitening (bleaching), distortion, uneven molding, or like defect to the bottle 2 resulted from the adhesion of the hydrogen peroxide can be prevented from causing.

When the preform 1 closely contacts the inner surface of the cavity C of the mold 4 to thereby form the bottle 2, the mold is opened at an instance contacting the wheel 21, and the bottle 2 is received by the gripper, not shown, disposed around the wheel 21.

The bottle 2 reaching the wheel 21 from the blow-molding machine 12 is inspected whether it is defective or not in the molded performance by an inspection device 35 arranged on the outer periphery of the wheel 21. The inspection device 35 may be provided with a light source and a camera for inspecting the top surface of the mouth portion 2 a of the molded bottle 2 is made to be flat or not.

The inspected bottle 2, which is judged to be defective, is rejected from the conveying path by a rejection device, not shown, and only an acceptable product is conveyed to the wheel 22.

The filling machine 13 is provided therein with the third conveying path as bottle conveying means, and such third conveying path is equipped with a line (train) of wheels 23, 24, 25, 26 and 27.

Around the outer periphery of the wheel 24, a number of filling nozzles 10 for filling the aseptic bottles 2 with the drink “a” are located so as to constitute a filler 39, and around the wheel 26, a capper 40 for applying the cap 3 (FIG. 2(G)) is also constituted to thereby seal each of the bottles 2 filled up with the drink “a”.

Since conventionally known filler and capper may be usable as such filler 39 and capper 40, detailed descriptions thereof will be omitted herein.

The chamber 41 c is located so as to surround the wheel 22, and this chamber 41 c functions as surrounding air shut-off chamber for shut off surrounding (atmosphere) air existing between the chamber 41 b and the chamber 41 d. Exhaust means like that composed of the filter 36 and the blower 37 and connected to the chamber 41 a shown in FIG. 3 is connected to this chamber 41 c to thereby exhaust outward the inner air in the chamber 41 d. Thus, gas or mist of the sterilizer and the cleaner generated within the chamber 41 d is rejected outside the chamber 41 c by performing the COP (Cleaning Out of Place) with respect to the interior of the chamber 41 d of the filling machine 13, and to thereby prevent the mist or line from flowing into the chamber 41 b of the blow-molding machine 12.

Hereunder, operation and/or function of the aseptic filling machine will be explained with reference to FIGS. 1 to 8.

First, the preforms 1 are conveyed toward the heating furnace 33 by the preform conveyer 14 and the line of the wheels 15, 16, 17.

At the time when the preforms 1 travel around the wheel 15 before the entering into the heating furnace 33, the hydrogen peroxide gas G or mist, or their mixture is supplied toward the preforms 1 from the sterilizer supplying nozzles 6, respectively.

Sequentially, the hot air P is blasted from the air nozzle 80 to the preform 1 at the time when the preform adhered with the hydrogen peroxide travels around the wheel 16. The hydrogen peroxide adhering to the preform 1 is activated by the heat of the hot air P, and bacteria and the like fungus adhering to the preform 1 can be sterilized. Moreover, the surplus hydrogen peroxide is removed by the blasting of the hot air P from the surface of the preform 1.

The blasting of the hot air P is performed by the air nozzle 81, as shown in FIG. 7, to thereby blast the foreign substance in the preform 1 outward thereof, and the blasted foreign substance may be recovered by the suction pipe 82. Further, as shown in FIG. 8, by arranging the air nozzle 81 and the preform 1 in an attitude inverted from the attitude shown in FIG. 7, the foreign substance in the preform 1 may be easily removed outward the preform 1.

Thereafter, the preform 1 is received by the spindle 43 above the endless chain 18 and then conveyed into the heating furnace 33.

The preform 1 in the heating furnace 33 is heated by the infrared heater 18 a to thereby evenly heat the entire of the preform, except the mouth portion 2 a, to a temperature suitable for the blow molding treatment.

When the preform 1 heated in the heating furnace 33 travels around the outer periphery of the wheel 20, the preform 1 is held by the mold 4 as shown in FIG. 2(D), and aseptic highly-pressurized air is blasted through the blow nozzle 5, and then, the preform 1 is expanded as a product bottle 2 within the cavity C of the mold 4.

The thus molded bottle 2 is taken out of the mold 4 after opening the mold 4 by the gripper 32 arranged around the wheel 21, and the bottle 2 is then inspected by the inspection device as to whether it is defective product or not.

Thereafter, the defective bottle 2 is rejected outward from the traveling line of the bottles by a rejecting device, not shown, and only a non-defective bottle 2 is guided and travels into the filling machine while being transferred to the line of the wheels 22, 23, 24, 25, 26 and 27.

Within the filling machine 13, the sterilized drink “a” fills the bottle 2 by the filling nozzle 10 of the filler 39 as shown in FIG. 2(F). The bottle 2 filled up with the drink “a” is applied with the cap 3 by the capper 40 to be sealed (see FIG. 2(G)), and discharged through the outlet port of the chamber 41 d.

As described hereinbefore, since, the filler 39 and the capper 40 are known ones, detailed descriptions thereof will be omitted herein.

Further, the interior of the chamber 41 d of the aseptic filling machine 13 is sterilized (SOP) by scattering the hydrogen peroxide gas or peracetic acid solution before production of package. Then, after the sterilization, by supplying the air through the aseptic filter, the interior of the chamber 41 d can be kept at positive pressure. As a result, although the air and the like in the chamber 41 d tends to flow toward the side of the blow-molding machine 12, since the surrounding air shut-off chamber 41 c is positioned between both the cambers 41 b and 41 d and such air and the like are discharged outward therefrom, high-humid air in the filling area of the chamber 41 d can be properly prevented from entering into the molding area in the chamber 41 b.

It may be possible to locate or arrange other various equipments and the like such as the sterilizer supply nozzle 6 and the air nozzle 80 for sterilizing the preform 1 for the sterilization of the bottle 2 to the portions of the wheels 22 and 23. In such case, since the sterilizer is exhausted outward from the surrounding air shut-off chamber 41 c by the exhausting means in the surrounding air shut-off chamber 41 c, the sterilizer can be shut off from flowing toward the side of the blow-molding machine 12.

Second Embodiment 2

According to the second embodiment 2, an aseptic package provided with a bottle 2 and a cap 3 such as shown in FIG. 13(K) can be manufactured as in the case of the first embodiment 1.

The bottle 2 is formed as an aseptic package through sterilizing process, molding process, drink filing process and sealing process as shown in FIG. 10 (A) to FIG. 13(K).

At first, the preforms 1 shown in FIG. 10(A) are continuously conveyed at a predetermined speed, and sterilizer gas G or mist, or their mixture is supplied to the preforms 1 now traveling.

Further, the sterilizer is supplied also in the like manner as in the first embodiment, and the hydrogen peroxide gas G or mist, or their mixture as sterilizer contacts and adheres to the inner and outer surfaces of the preform 1, thereby sterilizing bacteria or like fungus adhering to the surface of the preform 1 or giving damage thereto.

Further, it may be possible to preliminarily heat the preform by, for example, blasting heated air to the preform 1 just before the blasting of the gas G to the preform 1 as shown in FIG. 10(A).

The preform 1 supplied with the hydrogen peroxide is also supplied with the hot air P by the air nozzle 80 as like as in the first embodiment as shown in FIG. 10(B).

The hydrogen peroxide adhering to the surface of the preform 1 is activated by the heat of the hot air P, thereby sterilizing bacteria and the like fungus existing inside the preform 1. Furthermore, the hydrogen peroxide adhering to the preform 1 can be also removed promptly from the surface of the preform 1 by the blasting of the hot air P.

As shown in FIG. 10(C), the sterilized preform 1 is heated by the infrared heater 18 a and other heating means to a temperature suitable for the blow-molding treatment which will be performed thereafter. Such temperature is about 90° C. to 130° C. The preform 1 travels so that the mouth portion 2 a thereof moves through a position not facing the infrared heater 18 a to prevent the heat from being transferred to the mouth portion 2 a and not to be deformed by the heat.

As also shown in FIG. 10(C), when the preform 1 is heated, the preform 1 is supported by the spindle 43.

As shown in FIG. 15, a plurality of elastic members 43 b, each having a are embedded, and an umbrella-shaped member 43 a is attached to an outer portion of the spindle 43 as occasion demands.

When the lower portion of the spindle 43 is inserted into the mouth portion 2 a of the preform 1, the preform 1 is supported to the spindle 43 by the elastic deformation of the elastic members 43 b. In the case when the umbrella-shaped member 43 a is provided, the mouth portion 2 a of the preform 1 is covered by this umbrella-shaped member 43 a.

As also shown in FIG. 15, when the umbrella-shaped member 43 a is provided, a gap is formed to a portion between the inner surface of the mouth portion 2 a of the preform 1 and the lower portion of the spindle 43, and a portion between the outer surface of the mouth portion 2 a of the preform 1 and the umbrella-shaped member 43 a. Because of the formation of such gap, the air inside the preform 1 heated by the heat from the infrared heater 18 a changes to the hot air, which then flows outward of the preform 1 from the interior thereof through such gap while heating the mouth portion 2 a of the preform 1.

It is necessary to pay attention so as not to deform the preform 1 by the heat at the state of the preform for the reason that the sealing performance of bottle 2 is kept at the time when the bottle 2 is sealed by the cap 3.

The hot air passing through the gap heats the mouth portion 2 a, but attention should be paid so that the heating temperature is less than about 70° C., to prevent the deformation of the mouth portion 2 a. According to such heating to the mouth portion 2 a, very small amount of hydrogen peroxide remaining in the preform 1 is activated and the mouth portion 2 a is hence properly sterilized.

When the preform 1 is heated as mentioned above, the preform 1 is conveyed in a state suspended at a positively standing attitude by the insertion of the spindle 43 into the mouth portion 2 a thereof, preferably, while rotating together with the spindle 43 around the axis thereof. According to such operation, the preform 1 can be entirely, except the mouth portion 2 a, heated evenly by the infrared heater 18 a at a temperature about 90° C. to 130° C.

Further, the preform 1 may be conveyed in an inverted attitude.

The heated preform 1 is released from the spindle 43 as shown in FIG. 11(D), transferred to the gripper 32, and conveyed to the mold 4 for being subjected to the blow-molding treatment while blasting an aseptic air Q from the mouth portion 2 a as shown in FIG. 11(E). By such blasting of the aseptic air Q, the preform 1 can be moved into the mold 4 while keeping the aseptic condition.

Hot air may be used as such aseptic air Q. The preform 1 can be prevented from lowering in its temperature by the blasting of the hot air.

Further, as shown in FIG. 11(D), a cover 86 is disposed in form of a tunnel so as to surround the traveling path of the preform 1 at a portion at which the heated preform 1 is conveyed toward the mold 4. A top portion of the tunnel-shaped cover 86 covering the mouth portion 2 a of the preform 1 from the upper side thereof is formed as a roof having an inclining surface. To such top portion, nozzles 86 a through which the aseptic air Q is blasted toward the mouth portion 2 a of the preform 1 are provided in form of line or slit. According to such structure, the aseptic air Q can be effectively supplied to the preform 1, and the preform 1 travels within the chamber 41 h with the aseptic condition being maintained.

The preform 1 with the aseptic condition having been maintained by the blasting of the aseptic air Q is placed in the mold 4 as shown in FIG. 11(E).

The mold 4 is clamped (mold-clamped) while traveling at the same traveling speed as that of the preform 1, is subjected to the blow-molding treatment, and the mold 4 is thereafter opened.

As described above, the preform 1 is heated entirely, except the mouth portion 2 a thereof, in the heating process shown in FIG. 10(C) to a temperature suitable for the molding the preform 1. Accordingly, as shown in FIG. 11(E), when the extension rod 5 is inserted into the preform 1 after being placed in the mold 4, the preform 1 is extended within the mold 4 in the longitudinal direction thereof.

Subsequently, when aseptic air for, for example, primary and secondary blow-molding treatments is blasted sequentially into the preform 1 from the blow nozzle, not shown, the preform 1 is expanded till the preform 1 is produced as a product bottle 2 in the cavity C of the mold 4.

After the bottle 2 is molded in the mold 4 in the manner mentioned above, the mold 4 is opened while travelling, and the product bottle 2 is then taken out of the mold 4.

The bottle 2 after taken out of the mold 4 is conveyed till the hydrogen peroxide supply process shown in FIG. 12(G) starts while blasting the aseptic air Q from the mouth portion 2 a side. By the blasting of such aseptic air Q, the bottle 2 is conveyed directly below a hydrogen peroxide supply nozzle 93 so as not to be contaminated as possible as can by bacteria and the like fungus.

The aseptic air Q shown in FIG. 11(F) is preferably hot air. By blasting the hot air, since the temperature of the bottle 2 is prevented from lowering, the sterilizing effect by the hydrogen peroxide in the subsequent process can be expected to be improved.

Furthermore, as shown in FIG. 11(F), a cover 87 is provided in form of a tunnel so as to surround the traveling path of the bottle 2 at a portion at which the bottle 2 is conveyed toward the hydrogen peroxide supply nozzle 93 (see FIG. 12 (G)). A top portion of the tunnel-shaped cover 87 covering the mouth portion 2 a of the bottle 2 1 from the upper side thereof is formed as a roof having an inclining surface. To such top portion, nozzles 87 a through which the aseptic air Q is blasted toward the mouth portion 2 a of the bottle 2 or traveling path are provided in form of line or slit. According to such structure, the aseptic air Q can be effectively supplied to the preform 2, and the bottle 2 travels into the chambers 41 b and 41 c with the aseptic condition being maintained.

The bottle 2 blasted with the aseptic air Q is then sterilized by applying the hydrogen peroxide as sterilizer as shown in FIG. 12(G).

More specifically, the hydrogen peroxide mist M or gas G, or mixture thereof is blasted to the bottle 2 now being conveyed from the nozzle 93 for sterilization 93. The sterilizing nozzle 93 is arranged so as to face the mouth portion 2 a of the bottle 2. The hydrogen peroxide mist M or gas G, or mixture thereof drops downward from the tip end of the sterilizing nozzle 93 into the bottle 2 through the mouth portion 2 a thereof while contacting the inner surface of the bottle 2.

A tunnel 4 is provided to a portion on the traveling path of the bottle 2, and the hydrogen peroxide mist M or gas G, or mixture thereof discharged from the sterilizing nozzle 93 flows downward along the outer surface of the bottle 2 and stays inside the tunnel 44, so that the hydrogen peroxide mist M or gas G, or mixture thereof effectively adheres to the outer surface of the bottle 2.

The hydrogen peroxide mist M or gas G may be generated by the sterilizer gas generator 7 shown, for example, in FIG. 4.

The sterilizing nozzle 93 may be located to a predetermined position on the way of the conveying path or moved synchronously with the bottle 2.

As shown in FIG. 12(G), the mist M or gas G, or mixture thereof contacts the inner and outer surfaces of the bottle 2, and at such instance, since the heat applied to the bottle 2 in the state of the preform 1 and in the state shown in FIG. 11(F) remains, the bottle 2 is maintained with the predetermined temperature, thus being effectively sterilized.

This predetermined temperature is preferably 40° C. to 80° C. in the case of the preform 1 being formed of PET, and more preferably, 50° C. to 75° C. In the case of less than 40° C., the sterilizing performance is extremely degraded, and on the other hand, in the case of more than 80° C., the bottle may be contracted after the molding, thus being inconvenient.

After the blasting of the mist M or gas G, or mixture thereof, the bottle 2 is subjected to an air rinse treatment as shown in FIG. 12(H1). Such air rinsing is performed by blasting an aseptic air N from a nozzle 45 into the bottle 2, and the flow of such aseptic air N removes foreign substance, hydrogen peroxide or the like from the interior of the bottle 2. At that time, the bottle 2 keeps its positively standing attitude.

Preferably, an umbrella-shaped member 84 may be attached to the nozzle 45 as like as that shown in FIG. 9. The aseptic air N overflowing from the bottle 2 then flows toward the outer surface of the bottle 2 by the guidance of the inclination of the umbrella-shaped member 84, thereby rinsing the outer surface of the bottle 2.

Further, an air rinsing process shown in FIG. 12 (H2) may be adopted in place of the air rinsing process shown in FIG. 12(H1). In the air rinsing process shown in FIG. 12(H2), by blasting the aseptic air N into the bottle 2 through the mouth portion 2 a thereof now directed downward, the foreign substance and the like can drop outward through the mouth portion 2 a of the bottle 2. This air rinsing process shown in FIG. 12(H2) may be performed subsequently after the air rinsing process shown in FIG. 12(H1) by blasting the aseptic air N into the bottle 2. Furthermore, the umbrella-shaped member 84 may be attached to a nozzle 45 shown in FIG. 12(H2).

After the rinsing process, as occasion demands, the hydrogen peroxide adhering to the bottle 2 may be washed away and an aseptic air rinsing may be performed with aseptic water of normal temperature or hot water of 15° C. to 85° C. for removing the foreign substance and the like, as shown in FIG. 13(I). In such process, it may be preferred for one nozzle to be 5 L/min. to 15 L/min. for the cleaning rinsing time of 0.2 to 10 sec.

As described above, since the bottle 2 is sterilized furthermore by the hydrogen peroxide after the sterilization in the state of the preform 1, the using amount of the hydrogen peroxide can be reduced for each bottle 2, and hence, a further rinsing process using a hot water may be eliminated.

The hydrogen peroxide mist m or gas G used for the process shown in FIG. 12(G) will be explained hereunder.

In a case when the using amount of the hydrogen peroxide is converted into the hydrogen peroxide mist M for the sterilization of the bottle 2 only by the process shown in FIG. 12(G), the adhesion of the hydrogen peroxide of an amount of 50 μL/500 mL to 100 μL/500 mL thereof was needed for one bottle 2, whereas in a case when the preform 1 is sterilized by using the hydrogen peroxide of the using amount of 10 μL/500 mL to 50 μL/500 mL to be adhered to the bottle 2, it becomes possible to perform commercially available aseptic filling operation.

Furthermore, on the other hand, in a case when the using amount of the hydrogen peroxide is converted into the hydrogen peroxide gas G for the sterilization of the bottle 2 only by the process shown in FIG. 12(G), it was necessary to blast the hydrogen peroxide gas G of gas concentration of 5 mg/L to 10 mg/L to the bottle, whereas in a case of the present invention in which the preliminary sterilization due to the preliminary heating is performed to the preform 1, commercially available aseptic filling operation becomes possible by blasting the hydrogen peroxide gas of gas concentration of 1 mg/L to 5 mg/L.

In a case when the aseptic rising process is eliminated, the drink “a” fills the bottle 2 from the filling nozzle 10, as shown in FIG. 13(J), and as also shown in FIG. 13(K), the cap 3 as a lid is applied to the bottle 2 to be sealed, and the bottle 2 is produced as aseptic package.

Further, in this second embodiment 2, it may be possible to eliminate bottle sterilization processes corresponding to the processes shown in FIGS. 12 (G), (H1) and (H2), and the drink “a” fills the bottle 2 at a normal temperature under the aseptic condition after the sterilization process performed to the drink “a” itself.

Furthermore, it may be also possible to eliminate the bottle sterilization process mentioned above and to fill the bottle 2 with the drink “a” under a medium temperature of about 70° C. When the filling is performed at the medium temperature, existence of spore fungus within the drink “a” and the bottle 2 may be permitted, but mold, yeast or the like is sterilized by the heat possessed by the drink “a” itself, and the PET bottle 2 is not deformed. Accordingly, when the filling process is performed under the medium temperature, it is suitable for the drink “a” to be acidic drink or mineral water having a property for suppressing germination of the spore fungus.

An aseptic filling apparatus for carrying out the method of sterilizing the bottle 2 as mentioned above has a structure or configuration shown in FIG. 14, for example.

As shown in FIG. 14, the aseptic filling system is equipped with: the preform supplying machine 11 for supplying the preforms 1, each having a bottomed tubular shape and having the mouth portion 2 a (see FIG. 10 (A)), subsequently at a predetermined interval; the blow-molding machine 12; the sterilizing machine 88 for sterilizing the molded bottles 2; and the filling machine 13 for filling the bottles 2 with the drink “a” and sealing the bottles 2 with the caps 3, respectively, (see FIG. 13(K)).

In this aseptic filling system, the portion between the blow-molding machine 12 to the filling machine 13 is covered by the chambers 41 a, 41 b, 41 c 1, 41 c 2, 41 c 3, 41 d, 41 e, and 41 f.

The chamber 41 a is located to the position corresponding to the portion at which the sterilizer is applied to the preform, the chamber 41 b is located to the position corresponding to the portion at which the bottle 2 is molded, the chamber 41 c 1 is located to the position corresponding to the portion at which the bottle 2 is conveyed into the sterilizing machine 88, the chamber 41 c 2 is located to the position corresponding to the portion at which the sterilizer is applied to the bottle 2 and the bottle 2 is rinsed, and the chamber 41 d is located to the position corresponding to the portion at which the bottle 2 is filed up with the drink “a” as a content and then sealed.

The portion between the chamber 41 b to the chamber 41 c 1 is maintained as a clean room. In order to produce such clean room, positively pressurized aseptic air passing through the HEPA filter is supplied into the chambers 41 b to 41 c 1 before the production of an aseptic package. According to such manner, the interiors of the chambers 41 b to 41 c 1 are maintained to be clean, and it becomes possible to manufacture the bottle having high level of aseptic condition.

It may be possible to sterilize the interiors of the chambers 41 b to 41 c 1 by the hydrogen peroxide gas G of less than 10 mg/L before the blasting the aseptic air having positive pressure thereinto. In addition, the portions to which the preform 1 and the bottle 2 contact may be irradiated with an UV lamp (for ultraviolet ray sterilization), or portions to which the mold 4, the extension rod 5, the gripper 32 and the like contact may be wiped up with chemical agent including ethanol or hydrogen peroxide of the amount of 1%.

Between a portion from the preform supplying machine 11 to the filling machine 13, there are arranged a preform conveying means for conveying the preforms 1 on the first conveying path, a mold conveying means for conveying the molds 4 having cavities C, each in form of the product bottle 2, on the second conveying path connected to the first conveying path, and a bottle conveying means for conveying the bottles 2 molded by the molds 4 on the third conveying path connected to the second conveying path, while sterilizing and filling the bottles 2.

The first conveying path of the preform conveying means, the second conveying path of the mold conveying means and the third conveying path of the bottle conveying means are communicated with each other, and on the ways of these conveying paths, the grippers or like, not shown, for conveying the preforms 1 and the bottles 2 are located in the state of the bottle being held.

The preform conveying means is provided with a preform conveyer 14 on the way of the first conveying path for conveying the preforms 1 subsequently at a predetermined interval. The preform conveying means is further provided with a line of the wheels 15, 16 and 17 for receiving the preform 1 from the terminal end of the preform conveyer 14 and then conveying them, and the endless chain 18 for transferring the preforms 1 after the reception thereof.

Further, on the predetermined positions on the traveling path of the preform 1 in the wheel 15, there are also arranged the sterilizer gas generator 7 such as shown in FIG. 4 for generating the hydrogen peroxide gas G and the sterilizer supplying nozzle 6 such as shown in FIG. 10(A) for blasting the hydrogen peroxide gas G toward the preform 1.

Furthermore, on the predetermined position on the traveling path of the preform 1 in the wheel 16, there is also provided the air nozzle 80 (see FIG. 10(B)) fir activating the hydrogen peroxide adhering to the inner and outer surfaces of the preform 1 and discharging it out of the preform 1 by blasting the hot air P toward the preform 1.

As such air nozzle 80, the like nozzle shown in FIG. 5(A), (B) or FIG. 9 in connection with the first embodiment is usable.

As shown in FIG. 14, the wheels 15 and 16 are surrounded by the chamber 41 a, which is coupled with the exhaust means composed of the filter 36 decomposing the sterilizer such as hydrogen peroxide in the air inside the chamber 41 a and the blower 37 as like as the first embodiment as shown in FIG. 3. According to such arrangement, the flowing of the hydrogen peroxide into the adjacent blow-molding machine 12 can be prevented. Further, a heating furnace 33 for heating the preform 1 to a temperature suitable for molding the preform 1 is disposed to a portion, on the way of the first conveying path, from the wheel 17 contacting the wheel 16 to the wheel 19 contacting the second conveying path. This heating furnace 33 is also composed of as like as that in the first embodiment.

The preform 1 is evenly heated during the traveling within the heating furnace 33, and the preform 1 is heated entirely, except the mouth portion 2 a thereof, to a temperature of 90° C. to 130° C. suitable for the blow-molding treatment. The mouth portion 2 a is heated less than 70° C. so as not to damage the sealing performance when the cap 3 is applied.

The blow-molding machine 12 is arranged around the second conveying path. The blow-molding machine 12 has a structure as like as that of the first embodiment, which receives the preform 1 heated in the heating furnace 33 and molds the preform into the bottle 2.

Above the wheel 19 disposed between the first conveying path of the preform conveying means and the second conveying path of the mold conveying means, a cover 86 covering the mouth portion 2 a of the preform 1 traveling around this wheel 19 is provided in form of tunnel (FIG. 11(D)) so as to cover the mouth portion 2 a from the upper side. Aseptic air Q is blasted into this cover 86 toward the mouth portion 2 a of the preform 1. This aseptic air Q may be a part of the aseptic air P supplied from the aseptic air supplying device shown in FIG. 5(B) in the first embodiment.

According to such arrangement as described above, the preform 1 is surrounded by the chamber 41 b formed as a clean room and also covered by the cover 86 containing the aseptic air Q, and thus, the preform 1 is conveyed toward the blow-molding machine 12 with the high aseptic condition being maintained.

The mold 4 in the blow-molding machine 12 is opened at a position in contact to the wheel 21 as a starting end of the third conveying path, and the bottle 2 is received by the gripper, not shown, disposed around the wheel 21.

The bottle 2 conveyed out of the blow-molding machine 12 to the wheel 21 is inspected by the inspection device 35 disposed as occasion demands to the periphery of the wheel 21 to inspect the presence of the defect in the molding process. As the inspection device, the like one as used in the first embodiment may be used.

In the inspection by the inspection device 35, the bottle 2 judged as defective is rejected by a rejection device, not shown, from the conveying path, and only the bottle 2 judged to be acceptable is conveyed to the wheel 22.

Above the traveling path of the bottle 2 in the wheels 21, 22 and 89 on the way of the third conveying path, a cover 87 covering the mouth portion 2 a of the bottle 2 is provided in form of tunnel (FIG. 11(F)) so as to cover the mouth portion 2 a thereof from the upper side. Aseptic air Q blasted into this cover 87 may be a part of the aseptic air P supplied from the aseptic air supplying device shown in FIG. 5(B) in the first embodiment.

A sterilizer supplying nozzle 93 (see FIG. 12(G)) and an aseptic air supplying nozzle 45 (see FIG. 12 (H1) or (H2)) are provided in the line of the wheels 90, 91, 92 and 23 continuous to the wheel 89 on the way of the third conveying path.

More specifically, a plurality of sterilizer supplying nozzles 93 (for example, four nozzles in FIG. 14) are located to predetermined positions on the way of the bottle traveling path around the wheel 90, and the tunnels (each shown in FIG. 12(G)) through which the bottle 2 passes is also located in correspondence with the sterilizer supplying nozzle 93. The hydrogen peroxide mist M or gas G, or mixture thereof blasted from the sterilizer supplying nozzle 93 enters the bottle 2 and adheres to the inner surface of the bottle 2 to thereby form a thin film, and also flows along the outer surface of the bottle 2, which then fills the interior of the tunnel 44 and adheres to the outer surface of the bottle 2 to thereby form a thin film thereon.

Further, one or a plurality of aseptic air supplying nozzles 45 are located to predetermined positions on the way of the bottle traveling path around the wheel 92. The aseptic air N blasted from the aseptic supplying nozzle 45 contacts the inner and outer surfaces of the bottle 2 and removes the film of the surplus hydrogen peroxide adhering to the surface of the bottle 2. When the hot air is used as such aseptic air N, the hydrogen peroxide adhering to the inner and outer surfaces of the bottle 2 is activated, thereby enhancing the sterilizing effect.

Further, the sterilizer supplying nozzles 93 and the aseptic air supplying nozzles 44 may be located around the wheel 90 and 92, respectively, at the same pitch as that of the bottles 2 so that the hydrogen peroxide gas G and the aseptic air N will be blasted into the bottles 2 while being turned synchronously therewith.

The filler 39 and the capper 40 are located to positions on the way from the wheel 24, to which the wheel 23 is contacted, to the wheel 27 in the third conveying path.

More specifically, the filler 39 is constituted by a number of filling nozzles 10 (see FIG. 13(J)) located around the wheel 24 each for filling the bottle 2 with the drink “a”, and the capper 40 is for applying the cap 3 (see FIG. 13(K)) disposed around the wheel 26 to the bottle 2 filled up with the drink “a”.

The filler 39 and the capper 40 are ones identical to those of the first embodiment.

The periphery of the wheel 15 is surrounded by the chamber 41 a on the way of the first to third conveying paths. The peripheral portion from the wheel 16 to the wheel 21 is surrounded by the chamber 41 b. The peripheral portion from the wheel 22 and the wheel 89 is surrounded by the chamber 41 c 1. The peripheral portion from the wheel 90 to the wheel 23 is surrounded by the chamber 41 c 2. The peripheral portion from the wheel 24 to the wheel 27 is surrounded by the chamber 41 d.

Aseptic air cleaned by the HEPA filter, not shown, is always supplied into the chamber 41 b. Accordingly, the chamber 41 b is constituted as a clean room, thus preventing bacteria or like fungus from entering into the chamber 41 b.

The interiors of these chambers 41 a, 41 b, 41 c 1, 41 c 2, 41 d, 41 e and 41 f are sterilized by, for example, the COP (cleaning outside of place) treatment and the SOP (sterilizing outside of place) treatment, and thereafter, the sterilizer and the cleaner gas or mist in the chambers 41 a, 41 b, 41 c 2, 41 d, 41 e and 41 f are exhausted from the chambers 41 a, 41 b, 41 c 2, 41 d, 41 e and 41 f outside thereof by the exhausting means such as shown in FIG. 3, respectively. Then, by supplying aseptic air sterilized by a scrubber, filter and the like means into these chambers 41 a, 41 b, 41 c 2, 41 d, and 41 f, the aseptic condition within the chambers 41 a, 41 b, 41 c 2, 41 d, and 41 f can be maintained. Further, although the COP and the SOP treatments are necessarily performed for the chambers 41 d, 41 e and 41 f, it is not always necessary to perform such treatments for the chambers 41 a, 41 b, and 41 c 2.

Furthermore, the chambers 41 c 1 functions as a atmosphere shut-off chamber for shutting off the atmosphere between the chamber 41 b and the chamber 41 d, thereby preventing the cleaner gas or like generated by the COP and SOP treatments and the sterilizer mist or like generated in the chamber 41 c 2 from flowing into the chamber 41 b of the blow-molding machine 12 via the chamber 41 c 1.

Hereunder, the function or operation of the aseptic filling system will be explained with reference to FIGS. 10 to 15.

At first, the preform 1 is conveyed by the line of the wheels 15, 16 and 17 toward the heating furnace 33.

When the preform 1 travels around the wheel 15 before the entering into the heating furnace 33, the sterilizer gas G or mist M, or the mixture thereof is supplied to the preform 1 through the sterilizer supplying nozzle 6.

Subsequently, when the preform 1 to which the hydrogen peroxide adheres travels around the wheel 16, the hot air P is blasted from the air nozzle 80 to the preform 1. The hydrogen peroxide adhering to the preform 1 is activated by the heat of the hot air P to thereby sterilize the bacteria and the like fungus. In addition, the surplus hydrogen peroxide adhering to the surface of the preform 1 is removed by such heat of the hot air P.

Foreign substance in the preform 1 can be blasted out of the interior of the preform 1 by blasting the hot air P by means of the air nozzle 81 shown in FIG. 7, and the blasted foreign substance may be recovered by a suction tube 82. On the other hand, by arranging the air nozzle 81 and the preform 1 in the inverted attitude as shown in FIG. 8 with respect to the attitude shown in FIG. 7, the foreign substance in the preform 1 may be removed our of the preform 1.

Thereafter, the preform 1 is received by the spindle 43 on the endless chain 18 (see FIG. 10(C)), and then transferred to the heating furnace 33.

The preform 1 is then heated by the infrared heater 18 a within the heating furnace 33, and the preform 1 is entirely heated, except the mouth portion 2 a thereof, to the temperature suitable for the blow-molding treatment.

The preform 1 heated in the heating furnace 33 to the temperature suitable for the blow-molding treatment is blasted with the aseptic air Q while passing through the cover 86 during the traveling around the wheel 19. According to such blasting of the aseptic air Q, the preform 1 is conveyed to the blow-molding machine 12 while the aseptic condition being maintained. In the case where the aseptic air Q is hot air, the preform 1 can arrive at the blow-molding machine 12 with the temperature suitable for the blow-molding treatment being maintained.

When the preform 1 passes around the outer periphery of the wheel 20, the preform 1 is held by the mold 4 as shown in FIG. 11(E), and the highly pressurized aseptic air is blasted thereinto so that the preform 1 is expanded into the product bottle 2 within the cavity C of the mold 4.

The product bottle 2 is taken out of the mold 4 by the gripper of the wheel 21 after opening the mold 4, and thereafter, is subjected to the inspection by the inspection device 35 whether the molding defective is present or not.

The defective bottle 2 is removed from the conveying line by the rejecting device, not shown, and only the acceptable (non-defective) bottle 2 is transferred to the wheel 22 and then conveyed to the sterilizing machine 88.

Further, in the time when the bottle 2 travels from the wheel 21 to the wheel 89, the aseptic air Q is blasted to the bottle 2 while passing through the cover 87. Accordingly, the bottle 2 is conveyed to the sterilizing machine 88 with the aseptic condition being maintained. In the case where the aseptic air Q is hot air, the preform 1 can arrive at the sterilizing machine 88 while maintaining the temperature suitable for the sterilization.

The bottle 2 is sterilized by blasting the by hydrogen peroxide mist M or gas G, or the mixture thereof, as shown in FIG. 12(G)), while traveling around the wheel 90 within the sterilizing machine 88, and subsequently, the bottle 2 is air-rinsed by blasting the aseptic air N as shown in FIG. 12(H1) or (H2) while traveling around the wheel 92.

Thereafter, the bottle 2 enters the interior of the filing machine 13.

The bottle 2 in the filling machine 13 is filled up with the preliminarily sterilized drink “a” through the filling nozzle 10 of the filler 39 as shown in FIG. 13(J). The bottle 2 filled up with the drink “a” is applied with the cap 3 by the capper 40 to be sealed (see FIG. 13(K)), and then discharged out of the aseptic filling system through an outlet of the chamber 41 d.

It is further to be noted that, in this second embodiment, members or components same as or similar to those of other embodiments are added with the same reference numerals, and the duplicated explanations are hence omitted herein.

Third Embodiment 3

In this third embodiment, a sterilizer supplying nozzle 94 shown in FIG. 16 is used in place of the sterilizer supplying nozzle 6 shown in FIG. 10(A) in the process of supplying the sterilizer to the preform 1.

As shown in FIG. 16, the sterilizer supplying nozzle 94 is equipped with a pipe line 94 a extending in U-shape along the preform 1, and a discharge port 95 is formed to the pipe line 94 a so as to face the outer surface of the preform 1. A plurality of such discharge ports 95 are located at several portions so as to face the lower portions below the mouth portion 2 a of the preform 1 to thereby prevent the hydrogen peroxide as the sterilizer from entering into the preform 1.

The hydrogen peroxide gas G generated by a generator like the sterilizer gas generator 7 used in the second embodiment is blasted toward the outer surface of the preform from the discharge port 95 of the sterilizer supplying nozzle 94, and such gas G or mist, or the mixture thereof is blasted to the outer surface of the preform, except the mouth portion 2 a thereof. The hydrogen peroxide gas G or like does not enter the preform 1 and adheres to the outer surface of the preform 1. As a result, bacteria or like fungus existing on the outer surface of the preform 1 can be sterilized.

Further, the hydrogen peroxide existing in the pipe line 94 a of the sterilizer supplying nozzle 94 may be prevented from being condensed as dew by supplying hot air as the aseptic air.

Furthermore, such condensation as dew of the hydrogen peroxide in the pipe line 94 a may be also prevented by winding a ribbon heater around the pipe line 94 a.

In the third embodiment, the preform 1 having been subjected to the sterilizer supplying process by the sterilizer as shown in FIG. 10(A) is then subjected to the respective processes shown in FIGS. 10(B) and (C), and thereafter, subjected to the hot water rinsing process shown in FIG. 13(I). During such processes, the processes shown in FIG. 12(G), (H1) and (H2) are eliminated.

As shown in FIG. 13(I), in the hot water rinsing process, the bottle 2 has an inverted attitude with the mouth portion 2 a directed downward, and the aseptic hot water H is supplied into the bottle 2 by a hot water supplying nozzle 46 inserted into the bottle 2. The hot water H contacts entirely the inner surface of the bottle 2, and thereafter, is discharged out of the bottle 2 through the mouth portion 2 a thereof. The temperature of the hot water H is maintained to a temperature range at which the bottle 2 is not deformed, for example, about 70° C. to 85° C. A flow rate per one nozzle is 5 L/min. to 15 L/min., and it is desirable to set a cleaning rinsing time to be about 0.2 to 10 sec.

The bacteria and the like fungus in the bottle 2 can be sterilized by the hot water rinsing process mentioned above. The bacteria to be sterilized is, for example, fungus, yeast and the like, and spore forming fungus remains as it is.

Accordingly, the method of this third embodiment is preferably applicable to the manufacture of drink not requiring sterilization of spore germination fungus such as acidic drink, carbonated drink, mineral water or the like other than sub-acidity drink.

After the hot water rising treatment, the drink “a” fills the bottle 2 as shown in FIG. 13(J), and the cap 3 is applied to the bottle 2 to thereby seal the same as shown in FIG. 13(K).

Further, it is to be noted that, in this third embodiment, it may be possible to eliminate the hot water rinsing treatment to the bottle 2 (FIG. 13(I)), and to sterilize the interior of the bottle 2 by filling the bottle 2 with the drink “a” having a middle temperature of about 70° C. In the drink filling treatment at the middle temperature, the spore forming fungus permits to remain within the drink “a” and the bottle 2, but mold, yeast and the like fungus are sterilized by the heat of the drink “a”, and the PET bottle 2 can be prevented from being deformed. Accordingly, the drink filling operation at the middle temperature is suitable for a drink “a” such as acidic drink and mineral water having property of suppressing germination of the spore fungus.

Further, in the third embodiment, the same or like reference numerals are added to the same or like components or members in the other embodiments, and duplicated explanation will be omitted herein.

Fourth Embodiment 4

According to the fourth embodiment 4, an aseptic package provided with a bottle 2 and a cap 3 such as shown in FIG. 13(K) can be manufactured as in the case of the second embodiment 2.

The bottle 2 is formed as an aseptic package via the sterilizing process, molding process, drink filing process and sealing process as shown in FIG. 10 (A), (B), (C), FIG. 11(D), (E), FIG. 17, and FIG. 13(J), (K).

At first, the preforms 1 shown in FIG. 10(A) are continuously conveyed at a predetermined speed, and sterilizer gas G or mist, or their mixture is supplied to the preforms 1 now traveling.

Further, the preform 1 shown in FIG. 10(A) may be preliminarily heated by blasting the hot air to the preform 1 immediately before the blasting of the gas G to the preform 1.

The hot air P is supplied by the air nozzle 80 to the preform 1 to which the hydrogen peroxide has been supplied, as shown in FIG. 10(B).

The hydrogen peroxide adhering to the surface of the preform 1 is activated by the heat of the hot air P, and bacteria or like fungus inside the preform 1 can be sterilized. In addition, by blasting the hot air P, the hydrogen peroxide adhering to the surface of the preform 1 can be promptly removed therefrom.

As shown in FIG. 10(C), the sterilized preform 1 is then heated by the infrared heater 18 a or other heating means to a temperature suitable for the subsequent blow-molding treatment.

The heated preform 1 is, as shown in FIG. 11(D), released from the spindle 43, blasted with the aseptic air Q from the mouth portion side, and then, conveyed toward the mold 4 for the blow-molding treatment. According to such blasting of the aseptic air Q, the preform 1 is supplied to the mold 4 with the aseptic condition being maintained.

The preform 1 conveyed with the aseptic condition being maintained by the blasting of the aseptic air Q is conveyed into the mold 4 as shown in FIG. 11(E), into which the preform 1 is molded to a bottle 2.

The bottle 2 taken out of the mold 4 is conveyed while being blasted with the hydrogen peroxide mist M from the mouth portion side as shown in FIG. 17 till the bottle 2 reaches the portion for the drink filling operation shown in FIG. 13(J).

Further, in FIG. 17, the same reference numerals are added to the structural portions as that shown in FIGS. 4 and 5(B).

The hydrogen peroxide mist M is produced by a device shown in FIG. 17. That is, the bottle 2 is sterilized by passing the air flow by the blower 76 through the HEPA filter 77, heated by the heater 8, and fed to the outlet of the sterilizer gas generator 7 as heated wind (heated air). The hydrogen peroxide gas G generated by the sterilizer gas generator 7 is taken into the heated wind, then conveyed into the cover 87 through the nozzle 87 a, and thereafter changes as the hydrogen peroxide mist M.

The hydrogen peroxide mist M flows down to the bottle 2 now traveling inside the cover 87 from the upper side of the mouth portion 2 a and adheres to the outer surface of the bottle 2.

Furthermore, since the mist M fills the interior of the tunnel-shaped cover 87, the mist M adheres evenly to the inner and outer surfaces of bottle 2 in a state of an extremely thin film. The concentration of the hydrogen peroxide mist M is thinly diluted, and the inner and outer surfaces of the bottle 2 can be hence easily sterilized by the hydrogen peroxide component and the heat of the air-flow.

The air flow conveying the mist M provides positive pressure within the cover 87 to thereby block the invasion of the bacteria or like into the cover 87 and hence prevent the contamination of the bottle 2. Even if the bacteria invades into the cover 87, it is sterilized by the hydrogen peroxide.

After the bottle 2 passes through the cover 87, the drink “a” fills the bottle 2 through the filling nozzle 10 as shown in FIG. 13(J), and as shown in FIG. 13(K), the bottle 2 is applied with the cap 3 as a lid to thereby produce the bottle 2 as aseptic package.

The aseptic filling system for carrying out the method of sterilizing the bottle 2 has a configuration or structure shown in FIG. 18, for example.

As shown in FIG. 18, the aseptic filling system is provided with the preform supplying machine 11 for subsequently supplying the preforms 1, each having a bottomed-tubular shape and a mouth portion 2 a, at a predetermined interval (see FIG. 10(A)), the blow-molding machine 12, and the filling machine 13 which fills the molded bottle 2 (see FIG. 17) with the drink “a” (see FIG. 13(J)) and applies the to the bottle 2 to seal the same (see FIG. 13(K)).

In the aseptic filling system, the portion extending from the blow-molding machine 12 to the filling machine 13 is surrounded by the chambers 41 a, 41 b, 41 c, 41 d, 41 e and 41 f.

The chamber 41 a corresponds to the portion at which the sterilizer is supplied to the preform 1, the chamber 41 b corresponds to the portion at which the bottle 2 is molded, the chamber 41 c corresponds to the portion at which the bottle 2 is transferred to the content filling position, the chamber 41 d corresponds to the portion at which the drink “a” fills the bottle 2, and the chamber 41 e corresponds to the portion at which the bottle 2 is applied with the cap 3 to seal the bottle 2.

An outlet conveyer, not shown, is provided to an outlet portion of the bottle 2 in the chamber 41 e, and this outlet conveyer is surrounded by the chamber 41 f.

The portion extending from the chamber 41 b to the chamber 41 c is maintained as a clean room, and in order to form such clean room, the positively pressurized aseptic air suitable for the HEPA filter is supplied into the chambers 41 b and 41 c before the manufacture of the aseptic package. According to such arrangement, the interiors of the chambers 41 b and 41 c are maintained in the clean state, and it becomes possible to produce the bottle having high aseptic (i.e. sterilized) level.

Before the blasting of the positively pressurized aseptic air, the interior of the chambers 41 b and 41 c may be sterilized by the hydrogen peroxide gas of less than 10 mg/L. Furthermore, a portion to which the preform 1 or bottle 2 is contacted may be irradiated with an UV lamp (ultraviolet ray sterilization), or a portion to which the members or components such as mold 4, the extension rod 5, and the gripper 32 may be wiped by a chemical agent including ethanol or hydrogen peroxide of 1% by mass.

A preform conveying means, a mold conveying means and a bottle conveying means are located between the preform supplying machine 11 and the filling machine 13, in which the mold conveying means is for conveying the preforms 1 on the first conveying path, the mold conveying means is for conveying the mold 4 having a cavity “C” having a shape corresponding a final product of the bottle 2 (see FIG. 2(D)) on the second conveying path connected to the first conveying path, and the bottle conveying means is for conveying the bottle 2 molded by the mold 4 on the third conveying path connected to the second conveying path while sterilizing the bottle 2 and being filled with the drink “a”.

The first conveying path for the preform conveying means, the second conveying path for the mold conveying means and the third conveying path for the bottle conveying means are communicated with each other, and the grippers and like members, not shown, for holding and conveying the preforms 1 and the bottles 2 are provided on these conveying paths.

The structure or configuration between the first conveying path and the second conveying path is similar to that of the second embodiment, and the detailed explanation will be omitted herein.

The cover 87 (see FIG. 17) is provided in form of tunnel above the bottle traveling path in the wheels 21, 22 and 89 on the way of the third conveying path so as to cover the mouth portion 2 a of the bottle 2 from the upper side thereof.

An aseptic air supplying device such as shown in FIG. 17 is connected to a portion corresponding to the wheel 22 disposed substantially the inner central portion of the cover 87.

This aseptic air supplying device has a conduit extending from the blower 76 to the cover 87, and the HEPA filter 77 and the heater 78 are provided on the way of this conduit toward the downstream side. A sterilizer gas generator like the sterilizer gas generator 7 shown in FIG. 4 is provided between the heater 78 and the cover 87 on the way of the conduit.

According to the structure mentioned above, the air flow form the blower 76 is sterilized by the HEPA filter 77 and then heated by the heater 78, and the heated air formed as aseptic hot air flows inside the conduit, and flows into the cover 87 from the nozzle 87 a while being added with small amount of the hydrogen peroxide gas G frequently. The hydrogen peroxide gas G flows into the cover 87, and the bottle 2 travels in the cover 87 filled up with the hydrogen peroxide gas G.

The concentration of the hydrogen peroxide gas G is set to be less than 5 mg/L, and preferably, less than 3 mg/L. In a case when the hydrogen peroxide gas concentration is more than 5 mg/L, the hydrogen peroxide gas remains inside the bottle 2, and the gas concentration may exceed 0.5 ppm as the reference of FDA. However, if the bottle 2 has large volume, remaining amount of the hydrogen gas intends to become less, and in such case, the hydrogen peroxide gas concentration may be set to be higher than 5 mg/L.

Further, as shown in FIG. 18, the aseptic hot air from the aseptic air supplying device described above is heated further by another heater 96, and thereafter, supplied to the air nozzle 80, and also supplied into the cover 86 for the preform 1.

On the way of the third conveying path, the filler 39 and the capper 40 are disposed to portions from the wheel 24 continued to the wheel 89 to the wheel 27.

More specifically, the filler 39 is composed of a number of the filling nozzles 10 (see FIG. 13(J)) for filling the bottle 2 with the drink “a” around the wheel 24, and the capper 40 for sealing the bottle 2 filled up with the drink “a” by the cap 3 (see FIG. 13(K)) is provided around the wheel 26.

Next, the operation and function of the aseptic filling system will be explained with reference to FIGS. 17 and 18.

At first, the preforms 1 are conveyed toward the heating furnace 33 by the preform conveyer 14 and the lines of the wheels 15, 16, 17.

At the time when the preforms 1 travel around the wheel 15 before the entering of the preforms 1 into the heating furnace 33, the hydrogen peroxide gas G or mist, or their mixture is supplied toward the preforms 1 from the sterilizer supplying nozzles 6.

Sequentially, the hot air P is blasted from the air nozzle 80 to the preform 1 at the time when the preform adhered with the hydrogen peroxide travels around the wheel 16. The hydrogen peroxide adhering to the preform 1 is activated by the heat of the hot air P, and bacteria and like fungus adhering to the preform 1 can be sterilized. Moreover, the surplus hydrogen peroxide is removed by the blasting of the hot air P from the surface of the preform 1.

The blasting of the hot air P is performed by the air nozzle 81 shown in FIG. 7. The foreign substance existing in the preform 1 is blasted outward, and the thus blasted foreign substance may be recovered by the suction tube 82. Further, as shown in FIG. 8, the preform 1 and the air nozzle 82 may be inverted in attitude compared with those shown in FIG. 7 to thereby remove the foreign substance existing in the preform 1 outward.

Thereafter, the preform 1 is received by the spindle 43 (see FIG. 10 (C)) above the endless chain 18, and then conveyed into the heating furnace 33.

The preform 1 in the heating furnace 33 is heated by the infrared heater 18 a to thereby evenly heat the entire of the preform, except the mouth portion 2 a, to a temperature range suitable for the blow molding treatment.

When the preform 1 heated in the heating furnace 33 travels around the outer periphery of the wheel 19, the preform 1 is blasted with the aseptic air Q while passing through the interior of the cover 86 (see FIG. 11(D)). According to this operation, the preform 1 is conveyed to the blow-molding machine 12 while the aseptic condition being maintained. In the case of the aseptic air Q being the hot air, the preform 1 reaches to the blow-molding machine 12 while the temperature suitable for the molding treatment being maintained.

When the preform 1 travels around the outer periphery of the wheel 20, it is held by the mold 4 as shown in FIG. 11(E), and the preform 1 is expanded by blasting the highly pressurized aseptic air in the cavity C of the mold 4.

The thus molded bottle 2 is taken out of the mold 4 after opening the mold 4 by the gripper 32 of the wheel 21, and the bottle 2 is then inspected by the inspection to device 35 as to whether it is defective product or not.

Thereafter, the defective bottle 2 is rejected outward from the traveling line of the bottles by a rejecting device, not shown, and only an acceptable (non-defective) bottle 2 is transferred to the wheels 22 and 89 and conveyed on the downstream side.

When the bottle 2 travels from the wheel 21 to the wheel 89, the aseptic hot air Q added with fine amount of the hydrogen peroxide is blasted while passing through the cover 87. By the heat contained in the hot air Q and the hydrogen peroxide, bacteria and like fungus which may invade into the chamber 41 b can be sterilized, and the bottle 2 is thereby conveyed on the downstream side while maintaining the aseptic condition. Furthermore, the hydrogen peroxide is decomposed at a time of departure from the cover 87 or after the departure therefrom, and the bottle 2 is conveyed to the filling machine with no remaining of the hydrogen peroxide.

The bottle 2 passing out of the cover 87 travels toward the filling machine 13, in which the bottle 2 is filled with the drink “a” preliminarily sterilized by the filling nozzle 10 of the filler 39 as shown in FIG. 13(J). The bottle 2 filled up with the drink “a” is applied with the cap 3 by the capper 40 to be sealed (see FIG. 13(K)), and discharged outside the aseptic filling system through the outlet port of the chamber 41 d.

In this fourth embodiment, the like reference numerals are added to components and members corresponding to those of the other embodiments, and the detailed descriptions thereof will be omitted herein.

Fifth Embodiment 5

According to the fifth embodiment 4, an aseptic package provided with a bottle 2 and a cap 3 such as shown in FIG. 13(K) can be manufactured as in the case of the second embodiment 2.

The bottle 2 is formed as an aseptic package through sterilizing process, molding process, sterilizing process, drink filing process and sealing process as shown in FIG. 10 (A), (B), (C), FIG. 11(D), (E), FIG. 19, and FIG. 13(J), (K).

At first, the preforms 1 shown in FIG. 10(A) are continuously conveyed at a predetermined speed, and sterilizer gas G or mist, or their mixture is supplied to the preforms 1 now traveling.

Further, the preform 1 shown in FIG. 10(A) may be preliminarily heated by blasting the hot air to the preform 1 immediately before the blasting of the gas G to the preform 1.

The hot air P is supplied by the air nozzle 80 to the preform 1 to which the hydrogen peroxide has been supplied, as shown in FIG. 10(B).

The hydrogen peroxide adhering to the surface of the preform 1 is activated by the heat of the blasted hot air P, thereby sterilizing bacteria or like fungus inside the preform 1. In addition, by blasting the hot air P, the hydrogen peroxide adhering to the surface of the preform 1 can be promptly removed therefrom.

As shown in FIG. 10(C), the sterilized preform 1 is then heated by the infrared heater 18 a or other heating means to a temperature suitable for the subsequent blow-molding treatment.

The heated preform 1 is, as shown in FIG. 11 (D), released from the spindle 43, blasted with the aseptic air Q from the mouth portion side, and then conveyed toward the mold 4 for the blow-molding treatment. According to such blasting of the aseptic air Q, the preform 1 is supplied to the mold 4 with the aseptic condition being maintained.

The preform 1 conveyed with the aseptic condition being maintained by the blasting of the aseptic air Q is conveyed into the mold 4 as shown in FIG. 11(E), into which the preform 1 is molded to a bottle 2.

The bottle 2 taken out of the mold 4 is conveyed in the cover 87 till the bottle 2 reaches to a portion for the drink filling process. In a front stage of the cover 87, as shown in FIG. 19(F1), the aseptic hot air Q is blasted, in a middle stage of the cover 87, as shown in FIG. 19(F2), the bottle 2 is conveyed while the hydrogen peroxide gas G or mist M, or their mixture being blasted on the mouth portion side, and in a subsequent last stage of the cover 87, as shown in FIG. 19(F3), the bottle 2 is conveyed while being blasted with the aseptic hot air Q. In the case of the remaining hydrogen peroxide concentration in the bottle 2 is less than 0.5 ppm as the reference of the FDA, the normal temperature of hot air Q may be usable.

The bottle 2 is heated by blasting the aseptic hot air Q in the front stage of the cover 87 while the aseptic condition being maintained. According to this process, the bottle 2 travels in the middle stage of the cover while maintaining the predetermined temperature, and then, the hydrogen peroxide flowing into the middle stage is activated to thereby sterilize bacteria or like which may invade from the molding-machine side. When the bottle 2 passes the subsequent last stage of the cover 87, the surplus hydrogen peroxide adhering to the inner and outer surfaces of the bottle 2 is rinsed by the aseptic hot air Q and removed from the surfaces of the bottle 2. Thus, the bottle 2 is conveyed toward the next filling machine 23 while the aseptic condition being maintained.

When the bottle 2 passes the cover 87 and enters the filling machine 13, the drink “a” fills the bottle 2 from the filling nozzle 10 as shown in FIG. 13(J), and then, as shown in FIG. 13(K), the bottle 2 is applied and sealed with the cap 3 to thereby form the bottle 2 as aseptic package.

The aseptic filling system for carrying out the bottle sterilizing method has a configuration or structure shown in FIG. 20, for example.

As shown in FIG. 20, the aseptic filling system is equipped with the preform supplying machine 11 for supplying the preforms 1, each having a bottomed tubular shape and having the mouth portion 2 a (see FIG. 10 (A)), subsequently at a predetermined interval, the blow-molding machine 12, the sterilizing machine 88 for sterilizing the molded bottles 2 (see FIG. 19), and the filling machine 13 for filling the bottles 2 with the drink “a” (see FIG. 13(J)) and sealing the bottles 2 with the caps 3, respectively, (see FIG. 13(K)).

In this aseptic filling system, the portion between the blow-molding machine 12 and the filling machine 13 is covered by the chambers 41 a, 41 b, 41 c, 41 d, 41 e, and 41 f.

The chamber 41 a is located to the position corresponding to the portion at which the sterilizer is applied to the preform, the chamber 41 b is located to the position corresponding to the portion at which the bottle 2 is molded, the chamber 41 c is located to the position corresponding to the portion at which the bottle 2 is conveyed to the content filling position, and the chamber 41 d is located to the position corresponding to the portion at which the bottle 2 is up with the drink “a” as a content and then sealed.

The portion between the chamber 41 b and the chamber 41 c is maintained as a clean room. In order to produce such clean room, positively pressurized aseptic air passing through the HEPA filter, not shown, is supplied into the chambers 41 b to 41 c 1 before the production of an aseptic package. According to such manner, the interiors of the chambers 41 b to 41 c are maintained to be clean, and it becomes possible to manufacture the bottle 2 having high level of aseptic condition.

It may be possible to sterilize the interiors of the chambers 41 b to 41 c by the hydrogen peroxide gas G of less than 10 mg/L before blasting the aseptic positive pressure thereinto. In addition, the portions to which the preform 1 and the bottle 2 are contacted may be irradiated with an UV lamp (for ultraviolet ray sterilization), or portions to which the mold 4, the extension rod 5, the gripper 32 and the like are contacted may be wiped up with chemical agent including ethanol or hydrogen peroxide of the amount of 1%.

Between a portion from the preform supplying machine 11 to the filling machine 13, there are arranged a preform conveying means for conveying the preforms 1 on the first conveying path, a mold conveying means for conveying the molds 4 having cavities C (see FIG. 11(E)), each in form of the product bottle 2, on the second conveying path connected to the first conveying path, and a bottle conveying means for conveying the bottles 2 molded by the molds 4 on the third conveying path connected to the second conveying path, while sterilizing and filling the bottles 2.

The first conveying path of the preform conveying means, the second conveying path of the mold conveying means and the third conveying path of the bottle conveying means are communicated with each other, and on the ways of these conveying paths, the grippers, not shown, for conveying the preforms 1 and the bottles 2 are disposed in the state of the bottle being held.

The structure between the first conveying path and the second conveying path is the same as that of the second embodiment, and the details thereof will be omitted herein.

On the way of the third conveying path, the cover 87 (see FIG. 19) covering the bottle 2 from the upper side of the mouth portion 2 a thereof is provided in form of a tunnel.

As shown in FIG. 20, conduits extending from the aseptic air supply device are connected to inner the central portion of the cover 87, the upstream side portion and the downstream side portion thereof.

The aseptic air supply device is provided with a blower 76, an HEPA filter 77 and a heater 78 as like as the fourth embodiment.

However, different from the embodiment 4, a conduit extending from the heater 78 branches and extends as branch pipes toward the inner central portion, the upstream side portion and the downstream side portion of the cover 87. A sterilizer gas generator as like as the sterilizer gas generator 7 shown in FIG. 4 is provided to the branch pipe extending to the inner central portion of the cover 87, and a heater 98 is additionally provided on the slightly upstream side of the sterilizer gas generator 7.

According to the arrangement described above, the air flow from the blower 76 is sterilized by the HEPA filter 77, heated by the heater 78 so as to be formed as aseptic hot air, which then passes through the conduit and the branch pipes toward the interior of the cover 87.

A part, which flows into the branch pipe extending to the inner central portion of the cover 87, of the aseptic hot air flowing the conduit forms a gas flow of the hydrogen peroxide by adding the hydrogen peroxide gas G generated by the sterilizer gas generator 7 as shown in FIG. 19(F2) and flows in the central portion of the cover 87 from the nozzle 87 a as shown in FIG. 19(F3), in which the gas G changes to the mist M, which drops down toward the bottle 2 from the upper portion 2 a of the bottle 2 traveling inside the cover 87 and then adheres to the inner and outer surfaces of the bottle 2. The gas concentration of the hydrogen peroxide gas adhering to the bottle 2 is within 2 mg/L to 10 mg/L. Further, as shown in FIG. 19(F3), an exhaust pipe 99 is connected to the inner central portion of the cover 87, and the surplus hydrogen peroxide is discharged outward from the exhaust pipe 99.

A part, which flows into the branch pipe extending to the upstream side portion of the inner central portion of the cover 87, of the aseptic hot air flowing the conduit fills the upstream side portion to thereby prevent bacteria or like fungus from the outside of the cover 87 and maintain the cleaned condition in the bottle 2.

A part, which flows into the branch pipe extending to the downstream side portion of the inner central portion of the cover 87, of the aseptic hot air flowing the conduit fills the downstream side portion to thereby activate the hydrogen peroxide adhering to the bottle 2 and enhance the sterilizing performance. Further, the surplus hydrogen peroxide is decomposed and removed.

Further, as shown in FIG. 20, the aseptic hot air from the aseptic air supply device described above is further heated by another heater 96, and thereafter, supplied to the air nozzle 80 as well as within the cover 86 for the preform 1.

On the way of the third conveying path, the filler 39 and the capper 40 are located to portions between the wheel 24 subsequent to the wheel 89 and the wheel 27.

More specifically, a number of filling nozzles 10 (see FIG. 13(J) for filling the bottles 2 with the drink “a” are arranged around the wheel 26 to thereby constitute the filler 39, and around the wheel 26, the capper 40 for applying the cap 3 (see FIG. 13(K)) to each of the bottles 2 filled up with the drink “a” to thereby seal it.

The surrounding of the wheel 15 is surrounded by the chamber 41 a on the way of the first to third conveying paths. The peripheral portion from the wheel 16 to the wheel 21 is surrounded by the chamber 41 b. The peripheral portion of the wheel 22 and the wheel 89 is surrounded by the chamber 41 c. The peripheral portion from the wheel 24 to the wheel 27 is surrounded by the chamber 41 d.

The aseptic air cleaned by the HEPA filter, not shown, is always supplied into the chamber 41 b, and as a result, the chamber 41 b is constituted as a clean room into which the invasion of bacteria is blocked.

The interiors of these chambers 41 a to 41 f are subjected to the sterilization treatment by performing the COP and SOP treatments, and thereafter, the gas or mist of the sterilizer and the cleaner is discharged from these chambers by the exhaust means such as shown in FIG. 3 which are provided integrally with or respectively to these chambers 41 a to 41 f. Then, the aseptic air cleaned by the filter or like, not shown, is supplied into the respective chambers 41 a to 41 f to thereby maintain the aseptic condition therein.

On the other hand, the chambers 41 a, 41 b and 41 c are not portions to be splashed with product liquid such as drink. Since the interiors of the chambers 41 a and 41 c are exposed to a chemical agent during the manufacture, these chambers are free from the COP and SOP treatments with no risk of contamination by bacteria or like fungus.

Herein, supposing that a pressure inside the chamber 41 d by the blasting of the aseptic air is p3, and pressures in the inner central portion, the upstream side portion, and the downstream side portion of the cover 87 are respectively p1, p0, and p2, the pressures are adjusted to be p3>p2>p0>p1. More specifically, with reference to the atmospheric pressure, these pressures are set such that the pressure p3 is 30 to 100 Pa, the pressure p2 is 10 to 30 Pa, the pressure p0 is 0 to 10 Pa, and the pressure p1 is −30 to 0 Pa. According to such relationship between these pressures, the hydrogen peroxide supplied to the inner central portion of the cover 87 is blocked to flow into the upstream side portion and the downstream side portion thereof. Moreover, the air flow from the chamber 41 c side and the air containing the hydrogen peroxide can be perfectly blocked from entering the chamber 41 d in which the filling machine 39 is located.

Next, the operation and function of the aseptic filling system will be explained with reference to FIGS. 19 and 20.

At first, the preforms 1 are conveyed toward the heating furnace 33 by the preform conveyer 14 and the lines of the wheels 15, 16, 17.

At the time when the preforms 1 travel around the wheel 15, the hydrogen peroxide gas G or mist, or their mixture is supplied toward the preforms 1 from the sterilizer supplying nozzles 6 before the entering of the preforms 1 into the heating furnace 33.

Sequentially, the hot air P is blasted from the air nozzle 80 to the preform 1 at the time when the preform adhered with the hydrogen peroxide travels around the wheel 16. The hydrogen peroxide adhering to the preform 1 is activated by the heat of the hot air P, and bacteria and like fungus adhering to the preform 1 can be sterilized. In addition, the surplus hydrogen peroxide is removed by the blasting of the hot air P from the surface of the preform 1.

The blasting of the hot air P is performed by the air nozzle 81 shown in FIG. 7. The foreign substance existing in the preform 1 is blasted outward and the thus blasted foreign substance may be recovered by the suction tube 82. Further, as shown in FIG. 8, the preform 1 and the air nozzle 82 may be inverted in attitude compared with those shown in FIG. 7 to thereby remove the foreign substance existing in the preform 1 outward.

Thereafter, the preform 1 is received by the spindle 43 (see FIG. 10 (C)) above the endless chain 18, and then conveyed into the heating furnace 33.

The preform 1 in the heating furnace 33 is heated by the infrared heater 18 a to thereby evenly heat the entire of the preform, except the mouth portion 2 a, to a temperature range suitable for the blow molding treatment.

The preform 1 heated in the heating furnace 33 travels around the outer periphery of the wheel 19, and at that time, the preform 1 is blasted with the aseptic air Q while passing through the interior of the cover 86, and the preform 1 is conveyed to the blow-molding machine while the aseptic condition being maintained. In the case of the aseptic air Q being the hot air, the preform reaches to the blow-molding machine 12 while the temperature suitable for the molding treatment being maintained.

When the preform 1 travels around the outer periphery of the wheel 20, it is held by the mold 4 as shown in FIG. 11(E), and the preform 1 is expanded by blasting the highly pressurized aseptic air in the cavity C of the mold 4.

The thus molded bottle 2 is taken out of the mold 4 after opening the mold 4 by the gripper 32 arranged around the wheel 21, and the bottle 2 is then inspected by the inspection device 35 as to whether it is defective product or not.

Thereafter, the defective bottle 2 is rejected outward from the traveling line of the bottles by a rejecting device, not shown, and only a acceptable (non-defective) bottle 2 is transferred to the wheel 22 and then to the sterilizing machine 88.

When the bottle 2 travels from the wheel 21 to the wheel 89, the aseptic hot air Q is blasted while passing through the cover 87 on the upstream side as shown in FIG. 19(F1). According to such blasting, the bottle 2 travels toward the inner central portion while maintaining the aseptic condition. In the central portion, the bottle 2 is blasted with the hydrogen peroxide mist M. As a result, the hydrogen peroxide films are formed to the inner and outer surfaces of the bottle 2. Furthermore, in the downstream side portion, the aseptic air Q is blasted so as to activate the hydrogen peroxide adhering to the inner and outer surfaces of the bottle 2, and the surplus hydrogen peroxide is decomposed and then removed.

The bottle 2 travels toward the filling machine 13, in which the bottle 2 is filled with the drink “a” preliminarily sterilized by the filling nozzle 10 of the filler 39 as shown in FIG. 13(J). The bottle 2 filled up with the drink “a” is applied with the cap 3 by the capper 40 to be sealed (see FIG. 13(K)), and discharged outside the aseptic filling system through the outlet port of the chamber 41 d.

In this fifth embodiment, the like reference numerals are added to components and members corresponding to those of the other embodiments, and the detailed descriptions thereof will be omitted herein.

Sixth Embodiment 6

According to the sixth embodiment, an aseptic package provided with a bottle 2 applied with a cap 3 as like as the fifth embodiment shown in FIG. 13(K) can be manufactured.

Furthermore, the bottle 2 is manufactured as an aseptic package through sterilizing process, molding process, sterilizing process, drink filing process and sealing process as shown in FIG. 10 (A), (B), (C), FIG. 11(D), (E), FIG. 19 (F1), (F2), (F3) and FIG. 13(J), (K).

Although the aseptic filling system of this sixth embodiment is constructed likely as shown in FIG. 21, the hydrogen peroxide supplying method is different from that of the fifth embodiment with respect to the central portion in the cover 87.

That is, a plurality of generators, each as like as the sterilizer gas generator 7 shown in FIG. 4, are disposed to portions corresponding to the central portion of the cover 87. By supplying the hydrogen peroxide gas G generated by such sterilizer gas generators 7 to the central portion in the cover 87, the hydrogen peroxide mist M is atomized directly upward so that the hydrogen peroxide adheres to the inner and outer surfaces of the battle 2 now traveling in the cover 87. In FIG. 21, reference numeral 93 is a hydrogen peroxide supplying nozzle of the sterilizer gas generator 7.

In this sixth embodiment, the like reference numerals are added to components and members corresponding to those of the other embodiments, and the detailed descriptions thereof will be omitted herein.

REFERENCE NUMERAL

1—preform, 2—bottle, 6—nozzle, 6 a, 6 ab—pipe line, 9—evaporator, 30—umbrella-shaped member, 31—discharge port, 80—air nozzle, 80 a—blasting port, G—gas, P—hot air. 

1. A method of sterilizing a preform, comprising the steps of: sterilizing bacteria adhering to a preform made of resin by gasifying a sterilizer, discharging a sterilized gas toward a preform, now traveling, so as to adhere to the preform by discharging the sterilizer from a nozzle; activating the sterilizer adhering to the preform by blasting hot air to the preform; and sterilizing the bacteria adhering to the preform, and removing the sterilizer adhering to the preform, wherein the above-mentioned steps are performed subsequently in order.
 2. The preform sterilizing method according to claim 1, wherein the sterilizer is atomized in an evaporator to be gasified as a gas, and the gas is discharge toward the preform from a nozzle of an evaporator.
 3. The preform sterilizing method according to claim 1, wherein at least one of nozzles are disposed so as to face a preform traveling path and the sterilizer gas is blasted toward the preform from the nozzle.
 4. The preform sterilizing method according to claim 1, wherein flow of the sterilizer gas is branched into a plurality of flows, one of which flows toward a mouth portion of the preform and another of which flows toward an outer surface of the preform.
 5. The preform sterilizing method according to claim 4, wherein a surrounding of the one of sterilizer gas flow discharged from the nozzle is surrounded by an umbrella-shaped member, and gas or mist, or mixture thereof leaking from the mouth portion of the preform after entering the preform is guided by the umbrella-shaped member to the outer surface of the preform.
 6. The preform sterilizing method according to claim 1, wherein the sterilizer is a solution including at least 1% by mass of hydrogen peroxide component.
 7. The preform sterilizing method according to claim 1, wherein foreign substance existing in the preform is removed by a hot air.
 8. The preform sterilizing method according to claim 1, wherein an umbrella-shaped member covers above the mouth portion of the preform at a time when the preform is heated to a temperature for a blow-molding step.
 9. The preform sterilizing method according to claim 1, wherein an aseptic air is blasted to the mouth portion of the preform at a time when the preform is conveyed toward the mold after heating the preform to the temperature for the blow-molding step.
 10. An apparatus for sterilizing a preform comprising: a traveling unit that transfers a preform or a bottle from a supplying stage of the preform to a molding stage of the bottle; a nozzle that supplies a sterilizer gas to the preform; and an air nozzle that activates the sterilizer adhering to the preform by blasting a hot air to the preform and removes the sterilizer adhering to the preform therefrom, wherein the sterilizer gas supplying nozzle, and the hot air supplying nozzle are arranged in subsequently from an upstream side toward a downstream side of the traveling unit.
 11. The preform sterilizing apparatus according to claim 10, wherein the sterilizer atomized by a spray nozzle is gasified into a gas, and a nozzle is arranged to a front end portion of an evaporator from which the gas is discharged toward the preform.
 12. The preform sterilizing apparatus according to claim 10, wherein the nozzle that supplies the sterilizer is disposed along a preform traveling path, and the sterilizer gas is discharged toward the preform from the sterilizer gas supplying nozzle.
 13. The preform sterilizing apparatus according to claim 10, wherein the sterilizer gas supplying nozzle is branched into a plurality of pipe lines, one of the pipe lines has a discharge port facing an opening of the preform so that a discharge port faces the outer surface of the preform, and another pipe line extends toward the outer surface of the preform so that a discharge port thereof faces the outer surface of the preform.
 14. The preform sterilizing apparatus according to claim 13, wherein a surrounding of the one of the pipe line is surrounded by an umbrella-shaped member, and gas or mist, or mixture thereof leaking from the mouth portion of the preform after entering the preform is guided by the umbrella-shaped member to the outer surface of the preform.
 15. The preform sterilizing apparatus according to claim 10, wherein the sterilizer is a solution including at least 1% by mass of hydrogen peroxide component.
 16. The preform sterilizing apparatus according to claim 10, wherein the air nozzle is provided with a blasting port in form of slit for blasting the hot air and the blasting port extends along the traveling direction of the preform.
 17. The preform sterilizing apparatus according to claim 10, wherein a foreign substance exiting in the preform is removed by the hot air.
 18. The preform sterilizing apparatus according to claim 10, wherein an umbrella-shaped member that covers above the mouth portion of the preform is provided within the heating furnace.
 19. The preform sterilizing apparatus according to claim 10, wherein a cover is arranged on a way of a bottle traveling path along which the preform travels from the heating furnace to the mold, and an aseptic air is blasted from the cover side toward the mouth portion of the preform. 